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rs397508082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508082(-;-)
Make rs397508082(-;C)
Make rs397508082(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2587642
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508082
ebirs397508082
HLIrs397508082
Exacrs397508082
Varsomers397508082
Maprs397508082
PheGenIrs397508082
hapmaprs397508082
1000 genomesrs397508082
hgdprs397508082
ensemblrs397508082
gopubmedrs397508082
geneviewrs397508082
scholarrs397508082
googlers397508082
pharmgkbrs397508082
gwascentralrs397508082
openSNPrs397508082
23andMers397508082
23andMe allrs397508082
SNP Nexus

SNPshotrs397508082
SNPdbers397508082
MSV3drs397508082
GWAS Ctlgrs397508082
Max Magnitude0
ClinVar
Risk rs397508082(C;C)
Alt rs397508082(C;C)
Reference rs397508082(;)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype not provided
Reversed 0
HGVS NC_000011.9:g.2608872dupC
CLNSRC ClinVar
CLNACC RCV000045976.2, RCV000182279.2,