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rs199473439

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473439(A;A)
Make rs199473439(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947806
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473439
ebirs199473439
HLIrs199473439
Exacrs199473439
Varsomers199473439
Maprs199473439
PheGenIrs199473439
hapmaprs199473439
1000 genomesrs199473439
hgdprs199473439
ensemblrs199473439
gopubmedrs199473439
geneviewrs199473439
scholarrs199473439
googlers199473439
pharmgkbrs199473439
gwascentralrs199473439
openSNPrs199473439
23andMers199473439
23andMe allrs199473439
SNP Nexus

SNPshotrs199473439
SNPdbers199473439
MSV3drs199473439
GWAS Ctlgrs199473439
Max Magnitude0
ClinVar
Risk rs199473439(A;A)
Alt rs199473439(A;A)
Reference rs199473439(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.150644894C>T
CLNSRC ClinVar
CLNACC RCV000058162.2,