RS56264519 TMPRSS3

Health Risk Chr 21:42375787
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 8
Rare genetic deafness
Nonsyndromic genetic hearing loss
TMPRSS3-related disorder
Monogenic hearing loss
Autosomal recessive nonsyndromic hearing loss 8
Rare genetic deafness
Nonsyndromic genetic hearing loss
TMPRSS3-related disorder
Monogenic hearing loss
Other Variants in TMPRSS3
rs137852999 rs28939084 rs137853000 rs387906915 rs397517368 rs111033261 rs113747896 rs111033292 rs111033537 rs397517371
Ask Dr. Hemsworth about this variant