RS121918529 MEF2A

Health Risk Chr 15:99690400
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What This Variant Does
"[OMIM:?]
Associated Conditions
Coronary artery disease/myocardial infarction
Coronary artery disease
autosomal dominant
1
Coronary artery disease/myocardial infarction
Coronary artery disease
autosomal dominant
1
Other Variants in MEF2A
rs1297176531 rs121918531
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