Have questions? Visit https://www.reddit.com/r/SNPedia

rs199472770

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472770(A;G)
Make rs199472770(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2587579
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472770
ebirs199472770
HLIrs199472770
Exacrs199472770
Varsomers199472770
Maprs199472770
PheGenIrs199472770
hapmaprs199472770
1000 genomesrs199472770
hgdprs199472770
ensemblrs199472770
gopubmedrs199472770
geneviewrs199472770
scholarrs199472770
googlers199472770
pharmgkbrs199472770
gwascentralrs199472770
openSNPrs199472770
23andMers199472770
23andMe allrs199472770
SNP Nexus

SNPshotrs199472770
SNPdbers199472770
MSV3drs199472770
GWAS Ctlgrs199472770
Max Magnitude0
ClinVar
Risk rs199472770(G;G)
Alt rs199472770(G;G)
Reference rs199472770(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.2608809A>G
CLNSRC ClinVar
CLNACC RCV000057562.2,