RS28937588 KCNQ4

Health Risk Chr 1:40819893
Upload your DNA to see your genotype for this variant.
What This Variant Does
"deafness [OMIM:DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 2A
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 2A
Autosomal dominant nonsyndromic hearing loss 2A
Nonsyndromic genetic hearing loss
Rare genetic deafness
Autosomal dominant nonsyndromic hearing loss 2A
Other Variants in KCNQ4
rs80358277 rs28939710 rs80358271 rs80358278 rs80358276 rs80358272 rs80358279 rs80358273 rs80358269 rs1648206560
Ask Dr. Hemsworth about this variant