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rs199473008

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473008(A;G)
Make rs199473008(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150948857
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473008
ebirs199473008
HLIrs199473008
Exacrs199473008
Varsomers199473008
Maprs199473008
PheGenIrs199473008
hapmaprs199473008
1000 genomesrs199473008
hgdprs199473008
ensemblrs199473008
gopubmedrs199473008
geneviewrs199473008
scholarrs199473008
googlers199473008
pharmgkbrs199473008
gwascentralrs199473008
openSNPrs199473008
23andMers199473008
23andMe allrs199473008
SNP Nexus

SNPshotrs199473008
SNPdbers199473008
MSV3drs199473008
GWAS Ctlgrs199473008
Max Magnitude0
ClinVar
Risk rs199473008(G;G)
Alt rs199473008(G;G)
Reference rs199473008(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.150645945T>C
CLNSRC ClinVar
CLNACC RCV000058142.2,