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rs199473019

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199473019(A;A)
Make rs199473019(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947466
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199473019
ebirs199473019
HLIrs199473019
Exacrs199473019
Varsomers199473019
Maprs199473019
PheGenIrs199473019
hapmaprs199473019
1000 genomesrs199473019
hgdprs199473019
ensemblrs199473019
gopubmedrs199473019
geneviewrs199473019
scholarrs199473019
googlers199473019
pharmgkbrs199473019
gwascentralrs199473019
openSNPrs199473019
23andMers199473019
23andMe allrs199473019
SNP Nexus

SNPshotrs199473019
SNPdbers199473019
MSV3drs199473019
GWAS Ctlgrs199473019
Max Magnitude0
ClinVar
Risk rs199473019(A;A)
Alt rs199473019(A;A)
Reference rs199473019(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.150644554C>T
CLNSRC ClinVar
CLNACC RCV000058189.2,