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rs397508105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(C;C) 0 common in clinvar
Make rs397508105(-;-)
Make rs397508105(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2847865
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508105
ebirs397508105
HLIrs397508105
Exacrs397508105
Varsomers397508105
Maprs397508105
PheGenIrs397508105
hapmaprs397508105
1000 genomesrs397508105
hgdprs397508105
ensemblrs397508105
gopubmedrs397508105
geneviewrs397508105
scholarrs397508105
googlers397508105
pharmgkbrs397508105
gwascentralrs397508105
openSNPrs397508105
23andMers397508105
23andMe allrs397508105
SNP Nexus

SNPshotrs397508105
SNPdbers397508105
MSV3drs397508105
GWAS Ctlgrs397508105
Max Magnitude0
ClinVar
Risk rs397508105(CA,CC;CA,CC)
Alt rs397508105(CA,CC;CA,CC)
Reference rs397508105(C;C)
Significance Pathogenic
Disease Long QT syndrome 1 Long QT syndrome not provided
Variation info
Gene KCNQ1-AS1 KCNQ1
CLNDBN Long QT syndrome 1 Long QT syndrome, LQT1 subtype not provided
Reversed 0
HGVS NC_000011.9:g.2869095dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000003284.3, RCV000046040.2, RCV000182288.2,