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

rs397508095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508095(-;-)
Make rs397508095(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2768868
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508095
ebirs397508095
HLIrs397508095
Exacrs397508095
Varsomers397508095
Maprs397508095
PheGenIrs397508095
hapmaprs397508095
1000 genomesrs397508095
hgdprs397508095
ensemblrs397508095
gopubmedrs397508095
geneviewrs397508095
scholarrs397508095
googlers397508095
pharmgkbrs397508095
gwascentralrs397508095
openSNPrs397508095
23andMers397508095
23andMe allrs397508095
SNP Nexus

SNPshotrs397508095
SNPdbers397508095
MSV3drs397508095
GWAS Ctlgrs397508095
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397508095(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.2790098delC
CLNSRC ClinVar
CLNACC RCV000045992.2,