RS2227624 SERPINC1

Health Risk Chr 1:173914872
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What This Variant Does
"CLNSIG=255
Associated Conditions
Hereditary antithrombin deficiency
Thromboembolism
Deep venous thrombosis
Hereditary antithrombin deficiency
Thromboembolism
Deep venous thrombosis
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
SERPINC1 protein levels T OR: 0.71 6E-50 PubMed
TNN protein levels T OR: 0.46 6E-40 PubMed
Other Variants in SERPINC1
rs121909546 rs121909547 rs121909548 rs121909549 rs121909550 rs121909551 rs121909552 rs121909554 rs121909555 rs121909557
Ask Dr. Hemsworth about this variant