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rs121908590

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908590(G;T)
Make rs121908590(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position5045270
GeneKCNA5
is asnp
is mentioned by
dbSNPrs121908590
ebirs121908590
HLIrs121908590
Exacrs121908590
Varsomers121908590
Maprs121908590
PheGenIrs121908590
hapmaprs121908590
1000 genomesrs121908590
hgdprs121908590
ensemblrs121908590
gopubmedrs121908590
geneviewrs121908590
scholarrs121908590
googlers121908590
pharmgkbrs121908590
gwascentralrs121908590
openSNPrs121908590
23andMers121908590
23andMe allrs121908590
SNP Nexus

SNPshotrs121908590
SNPdbers121908590
MSV3drs121908590
GWAS Ctlgrs121908590
Max Magnitude0
OMIM176267
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908590(T;T)
Alt rs121908590(T;T)
Reference rs121908590(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Atrial fibrillation, familial, 7
Reversed 0
HGVS NC_000012.11:g.5154436G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014411.26,