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rs397508085

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508085(-;-)
Make rs397508085(-;G)
Make rs397508085(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2588752
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508085
ebirs397508085
HLIrs397508085
Exacrs397508085
Varsomers397508085
Maprs397508085
PheGenIrs397508085
hapmaprs397508085
1000 genomesrs397508085
hgdprs397508085
ensemblrs397508085
gopubmedrs397508085
geneviewrs397508085
scholarrs397508085
googlers397508085
pharmgkbrs397508085
gwascentralrs397508085
openSNPrs397508085
23andMers397508085
23andMe allrs397508085
SNP Nexus

SNPshotrs397508085
SNPdbers397508085
MSV3drs397508085
GWAS Ctlgrs397508085
Max Magnitude0
ClinVar
Risk rs397508085(G;G)
Alt rs397508085(G;G)
Reference rs397508085(;)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2609982dupG
CLNSRC ClinVar
CLNACC RCV000045979.2,