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rs199473507

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473507(A;G)
Make rs199473507(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952723
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473507
ebirs199473507
HLIrs199473507
Exacrs199473507
Varsomers199473507
Maprs199473507
PheGenIrs199473507
hapmaprs199473507
1000 genomesrs199473507
hgdprs199473507
ensemblrs199473507
gopubmedrs199473507
geneviewrs199473507
scholarrs199473507
googlers199473507
pharmgkbrs199473507
gwascentralrs199473507
openSNPrs199473507
23andMers199473507
23andMe allrs199473507
SNP Nexus

SNPshotrs199473507
SNPdbers199473507
MSV3drs199473507
GWAS Ctlgrs199473507
Max Magnitude0
ClinVar
Risk rs199473507(G;G)
Alt rs199473507(G;G)
Reference rs199473507(A;A)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150649811T>C
CLNSRC ClinVar
CLNACC RCV000057878.2,