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rs121434557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434557(G;T)
Make rs121434557(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position147758953
GeneGJA5, LOC102723321
is asnp
is mentioned by
dbSNPrs121434557
ebirs121434557
HLIrs121434557
Exacrs121434557
Varsomers121434557
Maprs121434557
PheGenIrs121434557
hapmaprs121434557
1000 genomesrs121434557
hgdprs121434557
ensemblrs121434557
gopubmedrs121434557
geneviewrs121434557
scholarrs121434557
googlers121434557
pharmgkbrs121434557
gwascentralrs121434557
openSNPrs121434557
23andMers121434557
23andMe allrs121434557
SNP Nexus

SNPshotrs121434557
SNPdbers121434557
MSV3drs121434557
GWAS Ctlgrs121434557
GMAF0.0004591
Max Magnitude0
OMIM121013
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434557(T;T)
Alt rs121434557(T;T)
Reference rs121434557(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, familial, 11
Reversed 1
HGVS NC_000001.10:g.147231061C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018521.23,