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rs199472777

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472777(A;G)
Make rs199472777(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2587634
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472777
ebirs199472777
HLIrs199472777
Exacrs199472777
Varsomers199472777
Maprs199472777
PheGenIrs199472777
hapmaprs199472777
1000 genomesrs199472777
hgdprs199472777
ensemblrs199472777
gopubmedrs199472777
geneviewrs199472777
scholarrs199472777
googlers199472777
pharmgkbrs199472777
gwascentralrs199472777
openSNPrs199472777
23andMers199472777
23andMe allrs199472777
SNP Nexus

SNPshotrs199472777
SNPdbers199472777
MSV3drs199472777
GWAS Ctlgrs199472777
Max Magnitude0
ClinVar
Risk rs199472777(G;G)
Alt rs199472777(G;G)
Reference rs199472777(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.2608864A>G
CLNSRC ClinVar
CLNACC RCV000057572.2,