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rs199473414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473414(C;G)
Make rs199473414(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974826
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473414
ebirs199473414
HLIrs199473414
Exacrs199473414
Varsomers199473414
Maprs199473414
PheGenIrs199473414
hapmaprs199473414
1000 genomesrs199473414
hgdprs199473414
ensemblrs199473414
gopubmedrs199473414
geneviewrs199473414
scholarrs199473414
googlers199473414
pharmgkbrs199473414
gwascentralrs199473414
openSNPrs199473414
23andMers199473414
23andMe allrs199473414
SNP Nexus

SNPshotrs199473414
SNPdbers199473414
MSV3drs199473414
GWAS Ctlgrs199473414
Max Magnitude0
ClinVar
Risk rs199473414(G;G)
Alt rs199473414(G;G)
Reference rs199473414(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.150671914G>C
CLNSRC ClinVar
CLNACC RCV000058057.2,