rs1799958(A;G)
From SNPedia
Considered to be a 'susceptibility' variant by some for SCAD; see text |
Is a | genotype |
of | rs1799958 |
Gene | ACADS |
Chromosome | 12 |
Position | 120,738,280 |
mentioned | by |
Magnitude | 1.5 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;G) | 1.5 | Considered to be a 'susceptibility' variant by some for SCAD; see text |
(G;G) | 0 | common in clinvar |
This is a very common variant; see text on main rs-page for discussion.