RS144948296 STRC

Health Risk Chr 15:43604750
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 16
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 16
Rare genetic deafness
Other Variants in STRC
rs786200882 rs786200883 rs139956283 rs727503442 rs199839039 rs727503443 rs376104748 rs727505074 rs727503449 rs141749062
Ask Dr. Hemsworth about this variant