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rs1799958(A;G)

From SNPedia
Considered to be a 'susceptibility' variant by some for SCAD; see text
Is agenotype
ofrs1799958
GeneACADS
Chromosome12
Position120,738,280
mentionedby
Magnitude1.5
ReputeBad
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.