Have questions? Visit https://www.reddit.com/r/SNPedia

rs397508084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508084(-;-)
Make rs397508084(-;A)
Make rs397508084(A;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588726
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508084
ebirs397508084
HLIrs397508084
Exacrs397508084
Varsomers397508084
Maprs397508084
PheGenIrs397508084
hapmaprs397508084
1000 genomesrs397508084
hgdprs397508084
ensemblrs397508084
gopubmedrs397508084
geneviewrs397508084
scholarrs397508084
googlers397508084
pharmgkbrs397508084
gwascentralrs397508084
openSNPrs397508084
23andMers397508084
23andMe allrs397508084
SNP Nexus

SNPshotrs397508084
SNPdbers397508084
MSV3drs397508084
GWAS Ctlgrs397508084
Max Magnitude0
ClinVar
Risk rs397508084(A;A)
Alt rs397508084(A;A)
Reference rs397508084(;)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2609956dupA
CLNSRC ClinVar
CLNACC RCV000045978.2,