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rs397508098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508098(A;A)
Make rs397508098(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2776985
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508098
ebirs397508098
HLIrs397508098
Exacrs397508098
Varsomers397508098
Maprs397508098
PheGenIrs397508098
hapmaprs397508098
1000 genomesrs397508098
hgdprs397508098
ensemblrs397508098
gopubmedrs397508098
geneviewrs397508098
scholarrs397508098
googlers397508098
pharmgkbrs397508098
gwascentralrs397508098
openSNPrs397508098
23andMers397508098
23andMe allrs397508098
SNP Nexus

SNPshotrs397508098
SNPdbers397508098
MSV3drs397508098
GWAS Ctlgrs397508098
Max Magnitude0
ClinVar
Risk rs397508098(A;A)
Alt rs397508098(A;A)
Reference rs397508098(G;G)
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.2798215G>A
CLNSRC ClinVar
CLNACC RCV000046013.2,