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

rs397508108

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508108(-;-)
Make rs397508108(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2445385
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508108
ebirs397508108
HLIrs397508108
Exacrs397508108
Varsomers397508108
Maprs397508108
PheGenIrs397508108
hapmaprs397508108
1000 genomesrs397508108
hgdprs397508108
ensemblrs397508108
gopubmedrs397508108
geneviewrs397508108
scholarrs397508108
googlers397508108
pharmgkbrs397508108
gwascentralrs397508108
openSNPrs397508108
23andMers397508108
23andMe allrs397508108
SNP Nexus

SNPshotrs397508108
SNPdbers397508108
MSV3drs397508108
GWAS Ctlgrs397508108
Max Magnitude0
ClinVar
Risk rs397508108(;)
Alt rs397508108(;)
Reference rs397508108(C;C)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2466615delC
CLNSRC ClinVar
CLNACC RCV000046045.2,