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rs121918529

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918529(C;T)
Make rs121918529(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position99690400
GeneMEF2A
is asnp
is mentioned by
dbSNPrs121918529
ebirs121918529
HLIrs121918529
Exacrs121918529
Varsomers121918529
Maprs121918529
PheGenIrs121918529
hapmaprs121918529
1000 genomesrs121918529
hgdprs121918529
ensemblrs121918529
gopubmedrs121918529
geneviewrs121918529
scholarrs121918529
googlers121918529
pharmgkbrs121918529
gwascentralrs121918529
openSNPrs121918529
23andMers121918529
23andMe allrs121918529
SNP Nexus

SNPshotrs121918529
SNPdbers121918529
MSV3drs121918529
GWAS Ctlgrs121918529
GMAF0.0004591
Max Magnitude0
OMIM600660
Desc
Variant0002
Relatedalso
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,