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rs121908592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908592(C;T)
Make rs121908592(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position5045874
GeneKCNA5
is asnp
is mentioned by
dbSNPrs121908592
ebirs121908592
HLIrs121908592
Exacrs121908592
Varsomers121908592
Maprs121908592
PheGenIrs121908592
hapmaprs121908592
1000 genomesrs121908592
hgdprs121908592
ensemblrs121908592
gopubmedrs121908592
geneviewrs121908592
scholarrs121908592
googlers121908592
pharmgkbrs121908592
gwascentralrs121908592
openSNPrs121908592
23andMers121908592
23andMe allrs121908592
SNP Nexus

SNPshotrs121908592
SNPdbers121908592
MSV3drs121908592
GWAS Ctlgrs121908592
Max Magnitude0
OMIM176267
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908592(T;T)
Alt rs121908592(T;T)
Reference rs121908592(C;C)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene KCNA5
CLNDBN Atrial fibrillation, familial, 7
Reversed 0
HGVS NC_000012.11:g.5155040C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014413.24,