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rs397508075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508075(C;T)
Make rs397508075(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2585254
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508075
ebirs397508075
HLIrs397508075
Exacrs397508075
Varsomers397508075
Maprs397508075
PheGenIrs397508075
hapmaprs397508075
1000 genomesrs397508075
hgdprs397508075
ensemblrs397508075
gopubmedrs397508075
geneviewrs397508075
scholarrs397508075
googlers397508075
pharmgkbrs397508075
gwascentralrs397508075
openSNPrs397508075
23andMers397508075
23andMe allrs397508075
SNP Nexus

SNPshotrs397508075
SNPdbers397508075
MSV3drs397508075
GWAS Ctlgrs397508075
Max Magnitude0
ClinVar
Risk rs397508075(T;T)
Alt rs397508075(T;T)
Reference rs397508075(C;C)
Significance Pathogenic
Disease Long QT syndrome Cardiac arrhythmia not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Cardiac arrhythmia not provided
Reversed 0
HGVS NC_000011.9:g.2606484C>T
CLNSRC ClinVar
CLNACC RCV000045954.2, RCV000182169.1, RCV000223715.1,