RS797044907 LRTOMT

Health Risk Chr 11:72108662
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 63
Inborn genetic diseases
Autosomal recessive nonsyndromic hearing loss 63
Other Variants in LRTOMT
rs1372399805 rs188715129 rs373088272 rs1565330066 rs1565331646 rs1298804148 rs774544844 rs1391956558 rs999863107 rs780468292
Ask Dr. Hemsworth about this variant