RS181949335 TMPRSS3

Health Risk Chr 21:42382101
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 8
Hearing impairment
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 8
Hearing impairment
Other Variants in TMPRSS3
rs137852999 rs28939084 rs137853000 rs387906915 rs397517368 rs111033261 rs113747896 rs111033292 rs111033537 rs397517371
Ask Dr. Hemsworth about this variant