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rs199472756

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472756(A;A)
Make rs199472756(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position2583486
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs199472756
ebirs199472756
HLIrs199472756
Exacrs199472756
Varsomers199472756
Maprs199472756
PheGenIrs199472756
hapmaprs199472756
1000 genomesrs199472756
hgdprs199472756
ensemblrs199472756
gopubmedrs199472756
geneviewrs199472756
scholarrs199472756
googlers199472756
pharmgkbrs199472756
gwascentralrs199472756
openSNPrs199472756
23andMers199472756
23andMe allrs199472756
SNP Nexus

SNPshotrs199472756
SNPdbers199472756
MSV3drs199472756
GWAS Ctlgrs199472756
Max Magnitude0
ClinVar
Risk rs199472756(A;A)
Alt rs199472756(A;A)
Reference rs199472756(G;G)
Significance Other
Disease Long QT syndrome Congenital long QT syndrome not provided
Variation info
Gene KCNQ1
CLNDBN Long QT syndrome, LQT1 subtype Congenital long QT syndrome not provided
Reversed 0
HGVS NC_000011.9:g.2604716G>A
CLNSRC ClinVar
CLNACC RCV000046184.2, RCV000057832.2, RCV000182150.2,