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rs199473486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473486(C;G)
Make rs199473486(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150977856
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473486
ebirs199473486
HLIrs199473486
Exacrs199473486
Varsomers199473486
Maprs199473486
PheGenIrs199473486
hapmaprs199473486
1000 genomesrs199473486
hgdprs199473486
ensemblrs199473486
gopubmedrs199473486
geneviewrs199473486
scholarrs199473486
googlers199473486
pharmgkbrs199473486
gwascentralrs199473486
openSNPrs199473486
23andMers199473486
23andMe allrs199473486
SNP Nexus

SNPshotrs199473486
SNPdbers199473486
MSV3drs199473486
GWAS Ctlgrs199473486
Max Magnitude0
ClinVar
Risk rs199473486(G;G)
Alt rs199473486(G;G)
Reference rs199473486(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150674944G>C
CLNSRC ClinVar
CLNACC RCV000058242.2,