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

rs199472768

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199472768(G;G)
Make rs199472768(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position2587576
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472768
ebirs199472768
HLIrs199472768
Exacrs199472768
Varsomers199472768
Maprs199472768
PheGenIrs199472768
hapmaprs199472768
1000 genomesrs199472768
hgdprs199472768
ensemblrs199472768
gopubmedrs199472768
geneviewrs199472768
scholarrs199472768
googlers199472768
pharmgkbrs199472768
gwascentralrs199472768
openSNPrs199472768
23andMers199472768
23andMe allrs199472768
SNP Nexus

SNPshotrs199472768
SNPdbers199472768
MSV3drs199472768
GWAS Ctlgrs199472768
Max Magnitude0
ClinVar
Risk rs199472768(C,G;C,G)
Alt rs199472768(C,G;C,G)
Reference rs199472768(T;T)
Significance Pathogenic
Disease SUDDEN INFANT DEATH SYNDROME Cardiac arrhythmia Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN SUDDEN INFANT DEATH SYNDROME Cardiac arrhythmia Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2608806T>C; NC_000011.9:g.2608806T>G
CLNSRC ClinVar
CLNACC RCV000057559.2, RCV000182179.1, RCV000057560.2,