RS139805921 TMPRSS3

Health Risk Chr 21:42388934 snv missense variant
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 8
Hearing impairment
TMPRSS3-related disorder
Autosomal recessive nonsyndromic hearing loss 8
Hearing impairment
TMPRSS3-related disorder
Population Frequencies
gnomAD ALL
100%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
0.1%
1kG EUR
100%
1kG SAS
100%
Other Variants in TMPRSS3
rs137852999 rs28939084 rs137853000 rs387906915 rs397517368 rs111033261 rs113747896 rs111033292 rs111033537 rs397517371
Ask Dr. Hemsworth about this variant