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rs397508109

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(A;A) 0 common in clinvar
Make rs397508109(-;-)
Make rs397508109(-;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position2445461
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508109
ebirs397508109
HLIrs397508109
Exacrs397508109
Varsomers397508109
Maprs397508109
PheGenIrs397508109
hapmaprs397508109
1000 genomesrs397508109
hgdprs397508109
ensemblrs397508109
gopubmedrs397508109
geneviewrs397508109
scholarrs397508109
googlers397508109
pharmgkbrs397508109
gwascentralrs397508109
openSNPrs397508109
23andMers397508109
23andMe allrs397508109
SNP Nexus

SNPshotrs397508109
SNPdbers397508109
MSV3drs397508109
GWAS Ctlgrs397508109
Max Magnitude0
ClinVar
Risk rs397508109(AA,AT;AA,AT)
Alt rs397508109(AA,AT;AA,AT)
Reference rs397508109(A;A)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2466691dupA
CLNSRC ClinVar
CLNACC RCV000046052.2,