rs121918530

Orientation

plus

Stabilized

plus

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

Make rs121918530(A;G)

Make rs121918530(G;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

99690352

Gene

MEF2A

is a	snp
is	mentioned by
dbSNP	rs121918530
dbSNP (classic)	rs121918530
ClinGen	rs121918530
ebi	rs121918530
HLI	rs121918530
Exac	rs121918530
Gnomad	rs121918530
Varsome	rs121918530
LitVar	rs121918530
Map	rs121918530
PheGenI	rs121918530
Biobank	rs121918530
1000 genomes	rs121918530
hgdp	rs121918530
ensembl	rs121918530
geneview	rs121918530
scholar	rs121918530
google	rs121918530
pharmgkb	rs121918530
gwascentral	rs121918530
openSNP	rs121918530
23andMe	rs121918530
SNPshot	rs121918530
SNPdbe	rs121918530
MSV3d	rs121918530
GWAS Ctlg	rs121918530

GMAF

0.0009183

Max Magnitude

0

OMIM	600660
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918530(G;G)
Alt	rs121918530(G;G)
Reference	Rs121918530(A;A)
Significance	Pathogenic
Disease	Coronary artery disease/myocardial infarction not specified
Variation	info
Gene	MEF2A
CLNDBN	Coronary artery disease/myocardial infarction not specified
Reversed	0
HGVS	NC_000015.9:g.100230557A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009506.4, RCV000420077.1,