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rs199472707

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472707(C;T)
Make rs199472707(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2571397
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472707
ebirs199472707
HLIrs199472707
Exacrs199472707
Varsomers199472707
Maprs199472707
PheGenIrs199472707
hapmaprs199472707
1000 genomesrs199472707
hgdprs199472707
ensemblrs199472707
gopubmedrs199472707
geneviewrs199472707
scholarrs199472707
googlers199472707
pharmgkbrs199472707
gwascentralrs199472707
openSNPrs199472707
23andMers199472707
23andMe allrs199472707
SNP Nexus

SNPshotrs199472707
SNPdbers199472707
MSV3drs199472707
GWAS Ctlgrs199472707
Max Magnitude0
ClinVar
Risk rs199472707(T;T)
Alt rs199472707(T;T)
Reference rs199472707(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2592627C>T
CLNSRC ClinVar
CLNACC RCV000057731.2,