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

rs199472863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472863(A;A)
Make rs199472863(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959656
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472863
ebirs199472863
HLIrs199472863
Exacrs199472863
Varsomers199472863
Maprs199472863
PheGenIrs199472863
hapmaprs199472863
1000 genomesrs199472863
hgdprs199472863
ensemblrs199472863
gopubmedrs199472863
geneviewrs199472863
scholarrs199472863
googlers199472863
pharmgkbrs199472863
gwascentralrs199472863
openSNPrs199472863
23andMers199472863
23andMe allrs199472863
SNP Nexus

SNPshotrs199472863
SNPdbers199472863
MSV3drs199472863
GWAS Ctlgrs199472863
Max Magnitude0
ClinVar
Risk rs199472863(A;A)
Alt rs199472863(A;A)
Reference rs199472863(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150656744C>T
CLNSRC ClinVar
CLNACC RCV000058232.2,