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rs199473014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473014(A;A)
Make rs199473014(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947684
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473014
ebirs199473014
HLIrs199473014
Exacrs199473014
Varsomers199473014
Maprs199473014
PheGenIrs199473014
hapmaprs199473014
1000 genomesrs199473014
hgdprs199473014
ensemblrs199473014
gopubmedrs199473014
geneviewrs199473014
scholarrs199473014
googlers199473014
pharmgkbrs199473014
gwascentralrs199473014
openSNPrs199473014
23andMers199473014
23andMe allrs199473014
SNP Nexus

SNPshotrs199473014
SNPdbers199473014
MSV3drs199473014
GWAS Ctlgrs199473014
Max Magnitude0
ClinVar
Risk rs199473014(A;A)
Alt rs199473014(A;A)
Reference rs199473014(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome Cardiac arrhythmia
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Cardiac arrhythmia
Reversed 1
HGVS NC_000007.13:g.150644772G>T
CLNSRC ClinVar
CLNACC RCV000058176.2, RCV000181899.1,