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rs397508086

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508086(-;-)
Make rs397508086(-;G)
Make rs397508086(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588754
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508086
ebirs397508086
HLIrs397508086
Exacrs397508086
Varsomers397508086
Maprs397508086
PheGenIrs397508086
hapmaprs397508086
1000 genomesrs397508086
hgdprs397508086
ensemblrs397508086
gopubmedrs397508086
geneviewrs397508086
scholarrs397508086
googlers397508086
pharmgkbrs397508086
gwascentralrs397508086
openSNPrs397508086
23andMers397508086
23andMe allrs397508086
SNP Nexus

SNPshotrs397508086
SNPdbers397508086
MSV3drs397508086
GWAS Ctlgrs397508086
Max Magnitude0
ClinVar
Risk rs397508086(G;G)
Alt rs397508086(G;G)
Reference rs397508086(;)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2609984dupG
CLNSRC ClinVar
CLNACC RCV000045980.2,