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rs199472796

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472796(A;A)
Make rs199472796(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2775990
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472796
ebirs199472796
HLIrs199472796
Exacrs199472796
Varsomers199472796
Maprs199472796
PheGenIrs199472796
hapmaprs199472796
1000 genomesrs199472796
hgdprs199472796
ensemblrs199472796
gopubmedrs199472796
geneviewrs199472796
scholarrs199472796
googlers199472796
pharmgkbrs199472796
gwascentralrs199472796
openSNPrs199472796
23andMers199472796
23andMe allrs199472796
SNP Nexus

SNPshotrs199472796
SNPdbers199472796
MSV3drs199472796
GWAS Ctlgrs199472796
Max Magnitude0
ClinVar
Risk rs199472796(A;A)
Alt rs199472796(A;A)
Reference rs199472796(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2797220G>A
CLNSRC ClinVar
CLNACC RCV000057606.2, RCV000182208.2,