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rs199473666

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473666(A;C)
Make rs199473666(C;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974798
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473666
ebirs199473666
HLIrs199473666
Exacrs199473666
Varsomers199473666
Maprs199473666
PheGenIrs199473666
hapmaprs199473666
1000 genomesrs199473666
hgdprs199473666
ensemblrs199473666
gopubmedrs199473666
geneviewrs199473666
scholarrs199473666
googlers199473666
pharmgkbrs199473666
gwascentralrs199473666
openSNPrs199473666
23andMers199473666
23andMe allrs199473666
SNP Nexus

SNPshotrs199473666
SNPdbers199473666
MSV3drs199473666
GWAS Ctlgrs199473666
Max Magnitude0
ClinVar
Risk rs199473666(C;C)
Alt rs199473666(C;C)
Reference rs199473666(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.150671886T>G
CLNSRC ClinVar
CLNACC RCV000058095.2,