RS1060499809 TRIOBP

Health Risk Chr 22:37724003
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 28
Autosomal recessive nonsyndromic hearing loss 28
Other Variants in TRIOBP
rs118204026 rs118204027 rs118204028 rs118204029 rs118204030 rs118204031 rs1601632909 rs200529550 rs200493962 rs397516554
Ask Dr. Hemsworth about this variant