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rs267607197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607197(A;A)
Make rs267607197(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2587690
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs267607197
ebirs267607197
HLIrs267607197
Exacrs267607197
Varsomers267607197
Maprs267607197
PheGenIrs267607197
hapmaprs267607197
1000 genomesrs267607197
hgdprs267607197
ensemblrs267607197
gopubmedrs267607197
geneviewrs267607197
scholarrs267607197
googlers267607197
pharmgkbrs267607197
gwascentralrs267607197
openSNPrs267607197
23andMers267607197
23andMe allrs267607197
SNP Nexus

SNPshotrs267607197
SNPdbers267607197
MSV3drs267607197
GWAS Ctlgrs267607197
Max Magnitude0
ClinVar
Risk rs267607197(A;A)
Alt rs267607197(A;A)
Reference rs267607197(G;G)
Significance Pathogenic
Disease Long QT syndrome 1
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome 1
Reversed 0
HGVS NC_000011.9:g.2608920G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003296.2,