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rs397508083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508083(-;-)
Make rs397508083(-;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588726
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508083
ebirs397508083
HLIrs397508083
Exacrs397508083
Varsomers397508083
Maprs397508083
PheGenIrs397508083
hapmaprs397508083
1000 genomesrs397508083
hgdprs397508083
ensemblrs397508083
gopubmedrs397508083
geneviewrs397508083
scholarrs397508083
googlers397508083
pharmgkbrs397508083
gwascentralrs397508083
openSNPrs397508083
23andMers397508083
23andMe allrs397508083
SNP Nexus

SNPshotrs397508083
SNPdbers397508083
MSV3drs397508083
GWAS Ctlgrs397508083
Max Magnitude0
ClinVar
Risk rs397508083(;)
Alt rs397508083(;)
Reference rs397508083(A;A)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2609956delA
CLNSRC ClinVar
CLNACC RCV000045977.2,