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rs199473027

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199473027(C;G)
Make rs199473027(G;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947011
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473027
ebirs199473027
HLIrs199473027
Exacrs199473027
Varsomers199473027
Maprs199473027
PheGenIrs199473027
hapmaprs199473027
1000 genomesrs199473027
hgdprs199473027
ensemblrs199473027
gopubmedrs199473027
geneviewrs199473027
scholarrs199473027
googlers199473027
pharmgkbrs199473027
gwascentralrs199473027
openSNPrs199473027
23andMers199473027
23andMe allrs199473027
SNP Nexus

SNPshotrs199473027
SNPdbers199473027
MSV3drs199473027
GWAS Ctlgrs199473027
Max Magnitude0
ClinVar
Risk rs199473027(G;G)
Alt rs199473027(G;G)
Reference rs199473027(C;C)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150644099G>C
CLNSRC ClinVar
CLNACC RCV000058208.2,