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rs397508114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508114(-;-)
Make rs397508114(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2570654
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508114
ebirs397508114
HLIrs397508114
Exacrs397508114
Varsomers397508114
Maprs397508114
PheGenIrs397508114
hapmaprs397508114
1000 genomesrs397508114
hgdprs397508114
ensemblrs397508114
gopubmedrs397508114
geneviewrs397508114
scholarrs397508114
googlers397508114
pharmgkbrs397508114
gwascentralrs397508114
openSNPrs397508114
23andMers397508114
23andMe allrs397508114
SNP Nexus

SNPshotrs397508114
SNPdbers397508114
MSV3drs397508114
GWAS Ctlgrs397508114
Max Magnitude0
ClinVar
Risk rs397508114(;)
Alt rs397508114(;)
Reference rs397508114(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.2591884delG
CLNSRC ClinVar
CLNACC RCV000046068.2,