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rs121918151(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs121918151
GenePROC, LOC105373608
Chromosome2
Position127,428,426
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Carrier of a thrombophilia due to protein C deficiency mutation
(T;T) 9 Complete protein-C deficiency; severe thrombophilia