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rs397508070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508070(A;A)
Make rs397508070(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2583546
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508070
ebirs397508070
HLIrs397508070
Exacrs397508070
Varsomers397508070
Maprs397508070
PheGenIrs397508070
hapmaprs397508070
1000 genomesrs397508070
hgdprs397508070
ensemblrs397508070
gopubmedrs397508070
geneviewrs397508070
scholarrs397508070
googlers397508070
pharmgkbrs397508070
gwascentralrs397508070
openSNPrs397508070
23andMers397508070
23andMe allrs397508070
SNP Nexus

SNPshotrs397508070
SNPdbers397508070
MSV3drs397508070
GWAS Ctlgrs397508070
Max Magnitude0
ClinVar
Risk rs397508070(A;A)
Alt rs397508070(A;A)
Reference rs397508070(G;G)
Significance Pathogenic
Disease Long QT syndrome not provided Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype not provided Long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2604776G>A
CLNSRC ClinVar
CLNACC RCV000045939.2, RCV000182161.1, RCV000190169.1,