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rs199473022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473022(A;A)
Make rs199473022(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947373
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473022
ebirs199473022
HLIrs199473022
Exacrs199473022
Varsomers199473022
Maprs199473022
PheGenIrs199473022
hapmaprs199473022
1000 genomesrs199473022
hgdprs199473022
ensemblrs199473022
gopubmedrs199473022
geneviewrs199473022
scholarrs199473022
googlers199473022
pharmgkbrs199473022
gwascentralrs199473022
openSNPrs199473022
23andMers199473022
23andMe allrs199473022
SNP Nexus

SNPshotrs199473022
SNPdbers199473022
MSV3drs199473022
GWAS Ctlgrs199473022
Max Magnitude0
ClinVar
Risk rs199473022(A;A)
Alt rs199473022(A;A)
Reference rs199473022(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.150644461C>T
CLNSRC ClinVar
CLNACC RCV000058197.2,