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rs199472836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472836(A;G)
Make rs199472836(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974890
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472836
ebirs199472836
HLIrs199472836
Exacrs199472836
Varsomers199472836
Maprs199472836
PheGenIrs199472836
hapmaprs199472836
1000 genomesrs199472836
hgdprs199472836
ensemblrs199472836
gopubmedrs199472836
geneviewrs199472836
scholarrs199472836
googlers199472836
pharmgkbrs199472836
gwascentralrs199472836
openSNPrs199472836
23andMers199472836
23andMe allrs199472836
SNP Nexus

SNPshotrs199472836
SNPdbers199472836
MSV3drs199472836
GWAS Ctlgrs199472836
Max Magnitude0
ClinVar
Risk rs199472836(G;G)
Alt rs199472836(G;G)
Reference rs199472836(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome not provided
Reversed 1
HGVS NC_000007.13:g.150671978T>C
CLNSRC ClinVar
CLNACC RCV000057889.2, RCV000181926.2,