RS201180712 SLC17A8

Health Risk Chr 12:100418127
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 25
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 25
Inborn genetic diseases
Other Variants in SLC17A8
rs121918339 rs373954823 rs138307707 rs140537845 rs11568530 rs141689561 rs374356596 rs141294063 rs748076639 rs2135999616
Ask Dr. Hemsworth about this variant