RS199839039 STRC

Health Risk Chr 15:43601395
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 16
Rare genetic deafness
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 16
Rare genetic deafness
Inborn genetic diseases
Other Variants in STRC
rs786200882 rs786200883 rs139956283 rs727503442 rs727503443 rs376104748 rs727505074 rs727503449 rs141749062 rs727503441
Ask Dr. Hemsworth about this variant