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rs199473670

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473670(A;A)
Make rs199473670(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947812
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473670
ebirs199473670
HLIrs199473670
Exacrs199473670
Varsomers199473670
Maprs199473670
PheGenIrs199473670
hapmaprs199473670
1000 genomesrs199473670
hgdprs199473670
ensemblrs199473670
gopubmedrs199473670
geneviewrs199473670
scholarrs199473670
googlers199473670
pharmgkbrs199473670
gwascentralrs199473670
openSNPrs199473670
23andMers199473670
23andMe allrs199473670
SNP Nexus

SNPshotrs199473670
SNPdbers199473670
MSV3drs199473670
GWAS Ctlgrs199473670
Max Magnitude0
ClinVar
Risk rs199473670(A;A)
Alt rs199473670(A;A)
Reference rs199473670(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.150644900C>T
CLNSRC ClinVar
CLNACC RCV000058160.2,