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rs397508104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508104(-;-)
Make rs397508104(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2847865
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508104
ebirs397508104
HLIrs397508104
Exacrs397508104
Varsomers397508104
Maprs397508104
PheGenIrs397508104
hapmaprs397508104
1000 genomesrs397508104
hgdprs397508104
ensemblrs397508104
gopubmedrs397508104
geneviewrs397508104
scholarrs397508104
googlers397508104
pharmgkbrs397508104
gwascentralrs397508104
openSNPrs397508104
23andMers397508104
23andMe allrs397508104
SNP Nexus

SNPshotrs397508104
SNPdbers397508104
MSV3drs397508104
GWAS Ctlgrs397508104
Max Magnitude0
ClinVar
Risk rs397508104(;)
Alt rs397508104(;)
Reference rs397508104(C;C)
Significance Pathogenic
Disease Long QT syndrome
Variation info
Gene KCNQ1-AS1 KCNQ1
CLNDBN Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2869095delC
CLNSRC ClinVar
CLNACC RCV000046039.3,