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rs397508077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTCA;TTCA) 0 common in clinvar
Make rs397508077(-;-)
Make rs397508077(-;TTCA)
ReferenceGRCh38 38.1/141
Chromosome11
Position2585303
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508077
ebirs397508077
HLIrs397508077
Exacrs397508077
Varsomers397508077
Maprs397508077
PheGenIrs397508077
hapmaprs397508077
1000 genomesrs397508077
hgdprs397508077
ensemblrs397508077
gopubmedrs397508077
geneviewrs397508077
scholarrs397508077
googlers397508077
pharmgkbrs397508077
gwascentralrs397508077
openSNPrs397508077
23andMers397508077
23andMe allrs397508077
SNP Nexus

SNPshotrs397508077
SNPdbers397508077
MSV3drs397508077
GWAS Ctlgrs397508077
Max Magnitude0
ClinVar
Risk rs397508077(;)
Alt rs397508077(;)
Reference rs397508077(TCAT;TCAT)
Significance Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype not provided
Reversed 0
HGVS NC_000011.9:g.2606533_2606536delTTCA
CLNSRC ClinVar
CLNACC RCV000045966.2, RCV000182278.2,