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rs121918530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918530(A;G)
Make rs121918530(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position99690352
GeneMEF2A
is asnp
is mentioned by
dbSNPrs121918530
ebirs121918530
HLIrs121918530
Exacrs121918530
Varsomers121918530
Maprs121918530
PheGenIrs121918530
hapmaprs121918530
1000 genomesrs121918530
hgdprs121918530
ensemblrs121918530
gopubmedrs121918530
geneviewrs121918530
scholarrs121918530
googlers121918530
pharmgkbrs121918530
gwascentralrs121918530
openSNPrs121918530
23andMers121918530
23andMe allrs121918530
SNP Nexus

SNPshotrs121918530
SNPdbers121918530
MSV3drs121918530
GWAS Ctlgrs121918530
GMAF0.0009183
Max Magnitude0
OMIM600660
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918530(G;G)
Alt rs121918530(G;G)
Reference rs121918530(A;A)
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.100230557A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009506.4,