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rs121434558

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs121434558(C;T)
Make rs121434558(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position147758977
GeneGJA5, LOC102723321
is asnp
is mentioned by
dbSNPrs121434558
ebirs121434558
HLIrs121434558
Exacrs121434558
Varsomers121434558
Maprs121434558
PheGenIrs121434558
hapmaprs121434558
1000 genomesrs121434558
hgdprs121434558
ensemblrs121434558
gopubmedrs121434558
geneviewrs121434558
scholarrs121434558
googlers121434558
pharmgkbrs121434558
gwascentralrs121434558
openSNPrs121434558
23andMers121434558
23andMe allrs121434558
SNP Nexus

SNPshotrs121434558
SNPdbers121434558
MSV3drs121434558
GWAS Ctlgrs121434558
Max Magnitude0
OMIM121013
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121434558(T;T)
Alt rs121434558(T;T)
Reference rs121434558(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene GJA5
CLNDBN Atrial fibrillation, somatic
Reversed 1
HGVS NC_000001.10:g.147231085G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018522.4,