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rs199472765

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472765(C;G)
Make rs199472765(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2585225
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472765
ebirs199472765
HLIrs199472765
Exacrs199472765
Varsomers199472765
Maprs199472765
PheGenIrs199472765
hapmaprs199472765
1000 genomesrs199472765
hgdprs199472765
ensemblrs199472765
gopubmedrs199472765
geneviewrs199472765
scholarrs199472765
googlers199472765
pharmgkbrs199472765
gwascentralrs199472765
openSNPrs199472765
23andMers199472765
23andMe allrs199472765
SNP Nexus

SNPshotrs199472765
SNPdbers199472765
MSV3drs199472765
GWAS Ctlgrs199472765
Max Magnitude0
ClinVar
Risk rs199472765(G;G)
Alt rs199472765(G;G)
Reference rs199472765(C;C)
Significance Pathogenic
Disease Long QT syndrome Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome Cardiac arrhythmia
Reversed 0
HGVS NC_000011.9:g.2606455C>G
CLNSRC ClinVar
CLNACC RCV000045946.2, RCV000057538.2, RCV000182330.1,