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rs121918531

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918531(A;A)
Make rs121918531(A;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position99690412
GeneMEF2A
is asnp
is mentioned by
dbSNPrs121918531
ebirs121918531
HLIrs121918531
Exacrs121918531
Varsomers121918531
Maprs121918531
PheGenIrs121918531
hapmaprs121918531
1000 genomesrs121918531
hgdprs121918531
ensemblrs121918531
gopubmedrs121918531
geneviewrs121918531
scholarrs121918531
googlers121918531
pharmgkbrs121918531
gwascentralrs121918531
openSNPrs121918531
23andMers121918531
23andMe allrs121918531
SNP Nexus

SNPshotrs121918531
SNPdbers121918531
MSV3drs121918531
GWAS Ctlgrs121918531
Max Magnitude0
OMIM600660
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918531(A;A)
Alt rs121918531(A;A)
Reference rs121918531(G;G)
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.100230617G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009507.2,