rs121918146(G;G)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs121918146 |
Gene | PROC, LOC105373608 |
Chromosome | 2 |
Position | 127,428,485 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
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 |