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rs397508099

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508099(-;-)
Make rs397508099(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position2777010
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs397508099
ebirs397508099
HLIrs397508099
Exacrs397508099
Varsomers397508099
Maprs397508099
PheGenIrs397508099
hapmaprs397508099
1000 genomesrs397508099
hgdprs397508099
ensemblrs397508099
gopubmedrs397508099
geneviewrs397508099
scholarrs397508099
googlers397508099
pharmgkbrs397508099
gwascentralrs397508099
openSNPrs397508099
23andMers397508099
23andMe allrs397508099
SNP Nexus

SNPshotrs397508099
SNPdbers397508099
MSV3drs397508099
GWAS Ctlgrs397508099
Max Magnitude0
ClinVar
Risk rs397508099(;)
Alt rs397508099(;)
Reference rs397508099(C;C)
Significance Untested
Disease Long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype
Reversed 0
HGVS NC_000011.9:g.2798240delC
CLNSRC ClinVar
CLNACC RCV000046020.2,