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rs199472769

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472769(C;C)
Make rs199472769(C;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2587577
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472769
ebirs199472769
HLIrs199472769
Exacrs199472769
Varsomers199472769
Maprs199472769
PheGenIrs199472769
hapmaprs199472769
1000 genomesrs199472769
hgdprs199472769
ensemblrs199472769
gopubmedrs199472769
geneviewrs199472769
scholarrs199472769
googlers199472769
pharmgkbrs199472769
gwascentralrs199472769
openSNPrs199472769
23andMers199472769
23andMe allrs199472769
SNP Nexus

SNPshotrs199472769
SNPdbers199472769
MSV3drs199472769
GWAS Ctlgrs199472769
Max Magnitude0
ClinVar
Risk rs199472769(C;C)
Alt rs199472769(C;C)
Reference Rs199472769(G;G)
Significance Untested
Disease Congenital long QT syndrome
Variation info
Gene KCNQ1
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000011.9:g.2608807G>C
CLNSRC ClinVar
CLNACC RCV000057561.3,