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rs121908593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908593(A;A)
Make rs121908593(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position5045975
GeneKCNA5
is asnp
is mentioned by
dbSNPrs121908593
ebirs121908593
HLIrs121908593
Exacrs121908593
Varsomers121908593
Maprs121908593
PheGenIrs121908593
hapmaprs121908593
1000 genomesrs121908593
hgdprs121908593
ensemblrs121908593
gopubmedrs121908593
geneviewrs121908593
scholarrs121908593
googlers121908593
pharmgkbrs121908593
gwascentralrs121908593
openSNPrs121908593
23andMers121908593
23andMe allrs121908593
SNP Nexus

SNPshotrs121908593
SNPdbers121908593
MSV3drs121908593
GWAS Ctlgrs121908593
Max Magnitude0
OMIM176267
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908593(A;A)
Alt rs121908593(A;A)
Reference rs121908593(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Atrial fibrillation, familial, 7
Reversed 0
HGVS NC_000012.11:g.5155141G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014414.26,