RS116310349 TMPRSS6

Health Risk Chr 22:37096088 snv missense variant
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Associated Conditions
Microcytic anemia
TMPRSS6-related disorder
Inborn genetic diseases
Microcytic anemia
TMPRSS6-related disorder
Inborn genetic diseases
Population Frequencies
gnomAD ALL
100%
1kG AFR
1%
1kG ALL
0.3%
1kG AMR
99.9%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in TMPRSS6
rs869320724 rs767094129 rs786205058 rs786205059 rs137853119 rs137853120 rs137853121 rs1384933966 rs137853122 rs137853123
Ask Dr. Hemsworth about this variant