USH2A Chromosome 1

Usherin
2089 variants 2089 Health Risk

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What This Gene Does
This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Info
Gene Group
"Fibronectin type III domain containing|USH2 complex"
Locus Type
gene with protein product
Location
1q41
Ensembl
ENSG00000042781
Associated Conditions (47)
Retinal dystrophy
Retinitis pigmentosa
Usher syndrome type 2A
Retinitis pigmentosa 39
Usher syndrome
Usher syndrome type 2
Inborn genetic diseases
USH2A-related disorder
Cone-rod dystrophy
Retinal disorder
Childhood onset hearing loss
Hearing impairment
Lung cancer
Stargardt-like macular dystrophy
Monogenic hearing loss
Rare genetic deafness
8 conditions
Progressive cone dystrophy (without rod involvement)
Clear cell carcinoma of kidney
Melanoma
+27 more conditions
Key Variants
All Variants (2089)
RSID Category Clinical Significance Conditions
RS1012665311 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS1026326311 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS1037325220 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa 39, Usher syndrome type 2A
RS1052375050 Health Risk Conflicting classifications of pathogenicity Usher syndrome, Usher syndrome
RS1064794034 Health Risk Conflicting classifications of pathogenicity
RS1064797129 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2, Usher syndrome type 2
RS1064797130 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2, Usher syndrome type 2
RS1064797137 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS111033248 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Usher syndrome type 2A, Inborn genetic diseases
RS111033275 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinal dystrophy, USH2A-related disorder
RS111033395 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2, Retinitis pigmentosa 39, Usher syndrome type 2
RS111033402 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa 39, Retinal dystrophy
RS111033419 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa 39, Usher syndrome
RS111033450 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, USH2A-related disorder, Retinal dystrophy
RS111033456 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa 39, Usher syndrome
RS111033479 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa, USH2A-related disorder
RS111033481 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa, Retinal dystrophy
RS111033508 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, USH2A-related disorder, Usher syndrome type 2A
RS111033514 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 39, Usher syndrome type 2A, Retinitis pigmentosa 39
RS111033515 Health Risk Conflicting classifications of pathogenicity
RS111033525 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Inborn genetic diseases, Usher syndrome type 2A
RS111033529 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 39, Usher syndrome type 2A
RS112120466 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Usher syndrome type 2A, USH2A-related disorder
RS113716139 Health Risk Conflicting classifications of pathogenicity
RS114116572 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Inborn genetic diseases, Usher syndrome type 2A
RS114194722 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Usher syndrome type 2A, USH2A-related disorder
RS115403785 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Usher syndrome type 2A
RS115494070 Health Risk Conflicting classifications of pathogenicity USH2A-related disorder, USH2A-related disorder
RS116367260 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa, Usher syndrome type 2A
RS1171264735 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 39, Usher syndrome
RS1172628170 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Usher syndrome type 2A, Retinitis pigmentosa
RS1173600555 Health Risk Conflicting classifications of pathogenicity
RS1176314553 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Usher syndrome type 2A
RS1188281491 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa 39, Usher syndrome type 2A
RS1230923403 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa 39, Usher syndrome type 2A
RS1231791432 Health Risk Conflicting classifications of pathogenicity
RS1234273599 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS1241034250 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinitis pigmentosa, Retinal dystrophy
RS1243406137 Health Risk Conflicting classifications of pathogenicity
RS1246009294 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Cone-rod dystrophy, Retinal dystrophy
RS1255592098 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 39, Retinitis pigmentosa 39
RS1268140508 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Retinitis pigmentosa 39, Retinal dystrophy
RS1294733964 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 39, Usher syndrome type 2A, Retinal dystrophy
RS1298852084 Health Risk Conflicting classifications of pathogenicity
RS1300984501 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 39, Usher syndrome type 2A, Retinitis pigmentosa 39
RS1310133198 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS1311224729 Health Risk Conflicting classifications of pathogenicity
RS1325681486 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Retinal disorder, Inborn genetic diseases
RS1341032857 Health Risk Conflicting classifications of pathogenicity Usher syndrome type 2A, Usher syndrome type 2A
RS1341186496 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
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