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rs199472850

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472850(C;C)
Make rs199472850(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974765
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472850
ebirs199472850
HLIrs199472850
Exacrs199472850
Varsomers199472850
Maprs199472850
PheGenIrs199472850
hapmaprs199472850
1000 genomesrs199472850
hgdprs199472850
ensemblrs199472850
gopubmedrs199472850
geneviewrs199472850
scholarrs199472850
googlers199472850
pharmgkbrs199472850
gwascentralrs199472850
openSNPrs199472850
23andMers199472850
23andMe allrs199472850
SNP Nexus

SNPshotrs199472850
SNPdbers199472850
MSV3drs199472850
GWAS Ctlgrs199472850
Max Magnitude0
ClinVar
Risk rs199472850(C;C)
Alt rs199472850(C;C)
Reference rs199472850(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.150671853C>G
CLNSRC ClinVar
CLNACC RCV000058134.2,