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rs397508100

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CGTC;CGTC) 0 common in clinvar
(TCCG;TCCG) 0 common in clinvar
Make rs397508100(-;-)
Make rs397508100(-;CGTC)
ReferenceGRCh38 38.1/141
Chromosome11
Position2777025
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508100
ClinGenrs397508100
ebirs397508100
HLIrs397508100
Exacrs397508100
Varsomers397508100
Maprs397508100
PheGenIrs397508100
hapmaprs397508100
1000 genomesrs397508100
hgdprs397508100
ensemblrs397508100
gopubmedrs397508100
geneviewrs397508100
scholarrs397508100
googlers397508100
pharmgkbrs397508100
gwascentralrs397508100
openSNPrs397508100
23andMers397508100
23andMe allrs397508100
SNP Nexus

SNPshotrs397508100
SNPdbers397508100
MSV3drs397508100
GWAS Ctlgrs397508100
Max Magnitude0
ClinVar
Risk rs397508100(-;-)
Alt rs397508100(-;-)
Reference Rs397508100(TCCG;TCCG)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2798255_2798258delCGTC
CLNSRC ClinVar
CLNACC RCV000046022.2,