rs121918529

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121918529(C;T)

Make rs121918529(T;T)

Reference

GRCh38 38.1/141

Chromosome

15

Position

99690400

Gene

MEF2A

is a	snp
is	mentioned by
dbSNP	rs121918529
dbSNP (classic)	rs121918529
ClinGen	rs121918529
ebi	rs121918529
HLI	rs121918529
Exac	rs121918529
Gnomad	rs121918529
Varsome	rs121918529
LitVar	rs121918529
Map	rs121918529
PheGenI	rs121918529
Biobank	rs121918529
1000 genomes	rs121918529
hgdp	rs121918529
ensembl	rs121918529
geneview	rs121918529
scholar	rs121918529
google	rs121918529
pharmgkb	rs121918529
gwascentral	rs121918529
openSNP	rs121918529
23andMe	rs121918529
SNPshot	rs121918529
SNPdbe	rs121918529
MSV3d	rs121918529
GWAS Ctlg	rs121918529

GMAF

0.0004591

Max Magnitude

0

OMIM	600660
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121918529(T;T)
Alt	rs121918529(T;T)
Reference	Rs121918529(C;C)
Significance	Pathogenic
Disease	Coronary artery disease/myocardial infarction
Variation	info
Gene	MEF2A
CLNDBN	Coronary artery disease/myocardial infarction
Reversed	0
HGVS	NC_000015.9:g.100230605C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009505.2,