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rs199472797

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472797(A;A)
Make rs199472797(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2775996
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472797
ebirs199472797
HLIrs199472797
Exacrs199472797
Varsomers199472797
Maprs199472797
PheGenIrs199472797
hapmaprs199472797
1000 genomesrs199472797
hgdprs199472797
ensemblrs199472797
gopubmedrs199472797
geneviewrs199472797
scholarrs199472797
googlers199472797
pharmgkbrs199472797
gwascentralrs199472797
openSNPrs199472797
23andMers199472797
23andMe allrs199472797
SNP Nexus

SNPshotrs199472797
SNPdbers199472797
MSV3drs199472797
GWAS Ctlgrs199472797
Max Magnitude0
ClinVar
Risk rs199472797(A;A)
Alt rs199472797(A;A)
Reference rs199472797(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2797226G>A
CLNSRC ClinVar
CLNACC RCV000057607.2,