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rs199472700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472700(A;G)
Make rs199472700(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2570742
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472700
ebirs199472700
HLIrs199472700
Exacrs199472700
Varsomers199472700
Maprs199472700
PheGenIrs199472700
hapmaprs199472700
1000 genomesrs199472700
hgdprs199472700
ensemblrs199472700
gopubmedrs199472700
geneviewrs199472700
scholarrs199472700
googlers199472700
pharmgkbrs199472700
gwascentralrs199472700
openSNPrs199472700
23andMers199472700
23andMe allrs199472700
SNP Nexus

SNPshotrs199472700
SNPdbers199472700
MSV3drs199472700
GWAS Ctlgrs199472700
Max Magnitude0
ClinVar
Risk rs199472700(G;G)
Alt rs199472700(G;G)
Reference rs199472700(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2591972A>G
CLNSRC ClinVar
CLNACC RCV000057715.2,