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rs397508078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508078(G;T)
Make rs397508078(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2585308
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508078
ebirs397508078
HLIrs397508078
Exacrs397508078
Varsomers397508078
Maprs397508078
PheGenIrs397508078
hapmaprs397508078
1000 genomesrs397508078
hgdprs397508078
ensemblrs397508078
gopubmedrs397508078
geneviewrs397508078
scholarrs397508078
googlers397508078
pharmgkbrs397508078
gwascentralrs397508078
openSNPrs397508078
23andMers397508078
23andMe allrs397508078
SNP Nexus

SNPshotrs397508078
SNPdbers397508078
MSV3drs397508078
GWAS Ctlgrs397508078
Max Magnitude0
ClinVar
Risk rs397508078(T;T)
Alt rs397508078(T;T)
Reference rs397508078(G;G)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2606538G>T
CLNSRC ClinVar
CLNACC RCV000045967.2,