RS374078257 KCNQ4

Health Risk Chr 1:40824225
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 2A
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 2A
Other Variants in KCNQ4
rs28937588 rs80358277 rs28939710 rs80358271 rs80358278 rs80358276 rs80358272 rs80358279 rs80358273 rs80358269
Ask Dr. Hemsworth about this variant