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rs121918146(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121918146
GenePROC, LOC105373608
Chromosome2
Position127,428,485
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 9 Complete protein-C deficiency; severe thrombophilia
(A;G) 3 Carrier of a thrombophilia due to protein C deficiency mutation
(G;G) 0 common in clinvar