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rs199472905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199472905(A;A)
Make rs199472905(A;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150952564
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472905
ebirs199472905
HLIrs199472905
Exacrs199472905
Varsomers199472905
Maprs199472905
PheGenIrs199472905
hapmaprs199472905
1000 genomesrs199472905
hgdprs199472905
ensemblrs199472905
gopubmedrs199472905
geneviewrs199472905
scholarrs199472905
googlers199472905
pharmgkbrs199472905
gwascentralrs199472905
openSNPrs199472905
23andMers199472905
23andMe allrs199472905
SNP Nexus

SNPshotrs199472905
SNPdbers199472905
MSV3drs199472905
GWAS Ctlgrs199472905
Max Magnitude0
ClinVar
Risk rs199472905(A;A)
Alt rs199472905(A;A)
Reference rs199472905(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.150649652G>T
CLNSRC ClinVar
CLNACC RCV000057905.2,