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rs199472736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472736(A;A)
Make rs199472736(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2572940
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472736
ebirs199472736
HLIrs199472736
Exacrs199472736
Varsomers199472736
Maprs199472736
PheGenIrs199472736
hapmaprs199472736
1000 genomesrs199472736
hgdprs199472736
ensemblrs199472736
gopubmedrs199472736
geneviewrs199472736
scholarrs199472736
googlers199472736
pharmgkbrs199472736
gwascentralrs199472736
openSNPrs199472736
23andMers199472736
23andMe allrs199472736
SNP Nexus

SNPshotrs199472736
SNPdbers199472736
MSV3drs199472736
GWAS Ctlgrs199472736
Max Magnitude0
ClinVar
Risk rs199472736(A;A)
Alt rs199472736(A;A)
Reference rs199472736(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.2594170G>A
CLNSRC ClinVar
CLNACC RCV000057784.2, RCV000182126.2,