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rs397508106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508106(-;-)
Make rs397508106(-;G)
Make rs397508106(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2847997
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508106
ebirs397508106
HLIrs397508106
Exacrs397508106
Varsomers397508106
Maprs397508106
PheGenIrs397508106
hapmaprs397508106
1000 genomesrs397508106
hgdprs397508106
ensemblrs397508106
gopubmedrs397508106
geneviewrs397508106
scholarrs397508106
googlers397508106
pharmgkbrs397508106
gwascentralrs397508106
openSNPrs397508106
23andMers397508106
23andMe allrs397508106
SNP Nexus

SNPshotrs397508106
SNPdbers397508106
MSV3drs397508106
GWAS Ctlgrs397508106
Max Magnitude0
ClinVar
Risk rs397508106(G;G)
Alt rs397508106(G;G)
Reference rs397508106(;)
Significance Pathogenic
Disease Long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNQ1-AS1 KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2869227dupG
CLNSRC ClinVar
CLNACC RCV000046042.2, RCV000182289.1,