| RS111033306 |
SLC26A4
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033307 |
SLC26A4
|
Health Risk |
Pathogenic |
Pendred syndrome, Rare genetic deafness |
| RS111033308 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033309 |
SLC26A4
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033310 |
SLC26A4
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 4, Pendred syndrome |
| RS111033311 |
SLC26A4
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033312 |
SLC26A4
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 4 |
| RS111033313 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Autosomal recessive nonsyndromic hearing loss 4, Pendred syndrome |
| RS111033314 |
SLC26A4
|
Health Risk |
Pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033316 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033317 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033318 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033319 |
MT-TS1
|
Health Risk |
Pathogenic |
Mitochondrial cytochrome c oxidase deficiency, Deafness |
| RS111033327 |
GJB2
|
Health Risk |
Conflicting classifications of pathogenicity |
Ichthyosis, hystrix-like |
| RS111033329 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 9, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033330 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Nonsyndromic genetic hearing loss, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033334 |
USH2A
|
Health Risk |
Pathogenic |
Usher syndrome type 2A, Retinitis pigmentosa 39 |
| RS111033335 |
GJB2
|
Health Risk |
Pathogenic/Likely pathogenic |
Hearing loss, Rare genetic deafness |
| RS111033337 |
MYO7A
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Usher syndrome type 1B |
| RS111033341 |
OTOF
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033342 |
OTOF
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Nonsyndromic genetic hearing loss |
| RS111033343 |
POU3F4
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033344 |
SLC26A4
|
Health Risk |
Conflicting classifications of pathogenicity |
— |
| RS111033345 |
POU3F4
|
Health Risk |
Pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033347 |
MYO7A
|
Health Risk |
Pathogenic |
Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2 |
| RS111033348 |
SLC26A4
|
Health Risk |
Pathogenic/Likely pathogenic |
Pendred syndrome, Autosomal recessive nonsyndromic hearing loss 4 |
| RS111033349 |
OTOF
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033351 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 9, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033352 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 9, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033360 |
GJB2
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 1A, 8 conditions |
| RS111033361 |
GJB2
|
Health Risk |
Likely pathogenic |
Nonsyndromic genetic hearing loss, Autosomal dominant nonsyndromic hearing loss 3A |
| RS111033363 |
PCDH15
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 1D, Usher syndrome type 1F |
| RS111033364 |
USH2A
|
Health Risk |
Pathogenic |
Usher syndrome type 2A, Hearing impairment |
| RS111033366 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
— |
| RS111033367 |
USH2A
|
Health Risk |
Pathogenic |
Usher syndrome type 2A, USH2A-related disorder |
| RS111033369 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 1D, Autosomal recessive nonsyndromic hearing loss 12 |
| RS111033370 |
OTOF
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033373 |
OTOF
|
Health Risk |
Pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033375 |
SLC26A4
|
Health Risk |
Conflicting classifications of pathogenicity |
— |
| RS111033376 |
MYO7A
|
Health Risk |
Pathogenic |
Usher syndrome type 1, Autosomal recessive nonsyndromic hearing loss 2 |
| RS111033379 |
USH2A
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Retinitis pigmentosa 39 |
| RS111033380 |
SLC26A4
|
Health Risk |
Pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 4 |
| RS111033382 |
USH2A
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Usher syndrome type 2A |
| RS111033383 |
OTOF
|
Health Risk |
Pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033384 |
OTOF
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033385 |
USH2A
|
Health Risk |
Pathogenic/Likely pathogenic |
Usher syndrome type 2A, Retinitis pigmentosa 39 |
| RS111033386 |
USH2A
|
Health Risk |
Pathogenic |
Rare genetic deafness, Retinal dystrophy |
| RS111033389 |
MYO7A
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033390 |
MYO7A
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033393 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 9, OTOF-related disorder |
| RS111033395 |
USH2A
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 2, Retinitis pigmentosa 39 |
| RS111033396 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 9, OTOF-related disorder |
| RS111033400 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033401 |
GJB2
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 1A |
| RS111033402 |
USH2A
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 2A, Retinitis pigmentosa 39 |
| RS111033403 |
MYO7A
|
Health Risk |
Pathogenic |
Rare genetic deafness, Usher syndrome type 1 |
| RS111033404 |
MYO7A
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033405 |
OTOF
|
Health Risk |
Pathogenic/Likely pathogenic |
Autosomal recessive nonsyndromic hearing loss 9, Rare genetic deafness |
| RS111033407 |
SLC26A4
|
Health Risk |
Pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033408 |
USH2A
|
Health Risk |
Pathogenic/Likely pathogenic |
Retinitis pigmentosa 39, Retinal dystrophy |
| RS111033412 |
USH2A
|
Health Risk |
Likely pathogenic |
Usher syndrome type 2A, Usher syndrome type 2A |
| RS111033414 |
USH2A
|
Health Risk |
Pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033415 |
MYO7A
|
Health Risk |
Pathogenic |
Rare genetic deafness, Usher syndrome type 1 |
| RS111033416 |
MYO7A
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 2, Usher syndrome type 1 |
| RS111033417 |
USH2A
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Retinal dystrophy |
| RS111033418 |
USH2A
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Usher syndrome type 2A |
| RS111033419 |
USH2A
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 2A, Retinitis pigmentosa 39 |
| RS111033420 |
GJB2
|
Health Risk |
Pathogenic/Likely pathogenic |
Rare genetic deafness, Autosomal recessive nonsyndromic hearing loss 1A |
| RS111033423 |
SLC26A4
|
Health Risk |
Conflicting classifications of pathogenicity |
Pendred syndrome, Autosomal recessive nonsyndromic hearing loss 4 |
| RS111033424 |
OTOF
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 9, Autosomal recessive nonsyndromic hearing loss 9 |
| RS111033426 |
MYO7A
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Usher syndrome type 1 |
| RS111033431 |
MYO6
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 37, Autosomal dominant nonsyndromic hearing loss 22 |
| RS111033433 |
MYO7A
|
Health Risk |
Pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033434 |
CLRN1
|
Health Risk |
Pathogenic |
Rare genetic deafness, Usher syndrome type 3A |
| RS111033436 |
PCDH15
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 1, Usher syndrome type 1F |
| RS111033437 |
MYO7A
|
Health Risk |
Likely pathogenic |
Autosomal dominant nonsyndromic hearing loss 11, Autosomal recessive nonsyndromic hearing loss 2 |
| RS111033439 |
USH2A
|
Health Risk |
Pathogenic/Likely pathogenic |
Usher syndrome type 2A, Retinitis pigmentosa 39 |
| RS111033443 |
SLC26A4
|
Health Risk |
Pathogenic/Likely pathogenic |
Pendred syndrome, Pendred syndrome |
| RS111033445 |
PCDH15
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 1, Usher syndrome type 1F |
| RS111033446 |
OTOF
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033447 |
OTOF
|
Health Risk |
Pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033448 |
MYO7A
|
Health Risk |
Pathogenic |
Rare genetic deafness, Hearing loss |
| RS111033449 |
PCDH15
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 1, Inborn genetic diseases |
| RS111033450 |
USH2A
|
Health Risk |
Conflicting classifications of pathogenicity |
Retinal dystrophy, USH2A-related disorder |
| RS111033451 |
GJB2
|
Health Risk |
Pathogenic/Likely pathogenic |
Autosomal recessive nonsyndromic hearing loss 1A, Rare genetic deafness |
| RS111033453 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 12, Usher syndrome type 1D |
| RS111033454 |
SLC26A4
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Pendred syndrome |
| RS111033455 |
OTOF
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033456 |
USH2A
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 2A, Retinitis pigmentosa 39 |
| RS111033457 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 12, Usher syndrome type 1D |
| RS111033458 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 12, Usher syndrome type 1D |
| RS111033459 |
WHRN
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 2D, Autosomal recessive nonsyndromic hearing loss 31 |
| RS111033461 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Autosomal recessive nonsyndromic hearing loss 12, Usher syndrome type 1D |
| RS111033472 |
USH2A
|
Health Risk |
Pathogenic |
— |
| RS111033473 |
CDH23
|
Health Risk |
Likely pathogenic |
Rare genetic deafness, Rare genetic deafness |
| RS111033475 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Inborn genetic diseases, Inborn genetic diseases |
| RS111033477 |
MYO7A
|
Health Risk |
Pathogenic/Likely pathogenic |
Retinal dystrophy, Ear malformation |
| RS111033478 |
OTOF
|
Health Risk |
Pathogenic |
— |
| RS111033479 |
USH2A
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 2A, Retinitis pigmentosa |
| RS111033480 |
CDH23
|
Health Risk |
Conflicting classifications of pathogenicity |
Usher syndrome type 1D, Usher syndrome |