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rs121908591

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908591(C;T)
Make rs121908591(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position5045727
GeneKCNA5
is asnp
is mentioned by
dbSNPrs121908591
ebirs121908591
HLIrs121908591
Exacrs121908591
Varsomers121908591
Maprs121908591
PheGenIrs121908591
hapmaprs121908591
1000 genomesrs121908591
hgdprs121908591
ensemblrs121908591
gopubmedrs121908591
geneviewrs121908591
scholarrs121908591
googlers121908591
pharmgkbrs121908591
gwascentralrs121908591
openSNPrs121908591
23andMers121908591
23andMe allrs121908591
SNP Nexus

SNPshotrs121908591
SNPdbers121908591
MSV3drs121908591
GWAS Ctlgrs121908591
GMAF0.001377
Max Magnitude0
OMIM176267
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908591(T;T)
Alt rs121908591(T;T)
Reference rs121908591(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Atrial fibrillation, familial, 7
Reversed 0
HGVS NC_000012.11:g.5154893C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014412.18,