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rs199472801

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472801(A;G)
Make rs199472801(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2776038
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472801
ebirs199472801
HLIrs199472801
Exacrs199472801
Varsomers199472801
Maprs199472801
PheGenIrs199472801
hapmaprs199472801
1000 genomesrs199472801
hgdprs199472801
ensemblrs199472801
gopubmedrs199472801
geneviewrs199472801
scholarrs199472801
googlers199472801
pharmgkbrs199472801
gwascentralrs199472801
openSNPrs199472801
23andMers199472801
23andMe allrs199472801
SNP Nexus

SNPshotrs199472801
SNPdbers199472801
MSV3drs199472801
GWAS Ctlgrs199472801
Max Magnitude0
ClinVar
Risk rs199472801(G;G)
Alt rs199472801(G;G)
Reference rs199472801(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.2797268A>G
CLNSRC ClinVar
CLNACC RCV000057615.2,