Have questions? Visit https://www.reddit.com/r/SNPedia

rs199473514

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473514(A;A)
Make rs199473514(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951829
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473514
ebirs199473514
HLIrs199473514
Exacrs199473514
Varsomers199473514
Maprs199473514
PheGenIrs199473514
hapmaprs199473514
1000 genomesrs199473514
hgdprs199473514
ensemblrs199473514
gopubmedrs199473514
geneviewrs199473514
scholarrs199473514
googlers199473514
pharmgkbrs199473514
gwascentralrs199473514
openSNPrs199473514
23andMers199473514
23andMe allrs199473514
SNP Nexus

SNPshotrs199473514
SNPdbers199473514
MSV3drs199473514
GWAS Ctlgrs199473514
Max Magnitude0
ClinVar
Risk rs199473514(A;A)
Alt rs199473514(A;A)
Reference rs199473514(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.150648917C>T
CLNSRC ClinVar
CLNACC RCV000057921.2,