RS111033261 TMPRSS3

Health Risk Chr 21:42380122 snv missense variant
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Associated Conditions
Autosomal recessive nonsyndromic hearing loss 8
Autosomal recessive nonsyndromic hearing loss 8
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
0.2%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.6%
1kG SAS
100%
Other Variants in TMPRSS3
rs137852999 rs28939084 rs137853000 rs387906915 rs397517368 rs113747896 rs111033292 rs111033537 rs397517371 rs56178910
Ask Dr. Hemsworth about this variant