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rs199473510

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473510(G;T)
Make rs199473510(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952616
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473510
ebirs199473510
HLIrs199473510
Exacrs199473510
Varsomers199473510
Maprs199473510
PheGenIrs199473510
hapmaprs199473510
1000 genomesrs199473510
hgdprs199473510
ensemblrs199473510
gopubmedrs199473510
geneviewrs199473510
scholarrs199473510
googlers199473510
pharmgkbrs199473510
gwascentralrs199473510
openSNPrs199473510
23andMers199473510
23andMe allrs199473510
SNP Nexus

SNPshotrs199473510
SNPdbers199473510
MSV3drs199473510
GWAS Ctlgrs199473510
Max Magnitude0
ClinVar
Risk rs199473510(T;T)
Alt rs199473510(T;T)
Reference rs199473510(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.150649704C>A
CLNSRC ClinVar
CLNACC RCV000057898.2,