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rs397508081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508081(-;-)
Make rs397508081(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2587630
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508081
ebirs397508081
HLIrs397508081
Exacrs397508081
Varsomers397508081
Maprs397508081
PheGenIrs397508081
hapmaprs397508081
1000 genomesrs397508081
hgdprs397508081
ensemblrs397508081
gopubmedrs397508081
geneviewrs397508081
scholarrs397508081
googlers397508081
pharmgkbrs397508081
gwascentralrs397508081
openSNPrs397508081
23andMers397508081
23andMe allrs397508081
SNP Nexus

SNPshotrs397508081
SNPdbers397508081
MSV3drs397508081
GWAS Ctlgrs397508081
Max Magnitude0
ClinVar
Risk rs397508081(;)
Alt rs397508081(;)
Reference rs397508081(C;C)
Significance Untested
Disease Jervell and Lange-Nielsen syndrome 1
Variation info
Gene KCNQ1
CLNDBN Jervell and Lange-Nielsen syndrome 1
Reversed 0
HGVS NC_000011.9:g.2608860delC
CLNSRC ClinVar
CLNACC RCV000045975.2,