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rs199472825

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199472825(A;C)
Make rs199472825(C;C)
ReferenceGRCh38 38.1/142
Chromosome7
Position150977867
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472825
ebirs199472825
HLIrs199472825
Exacrs199472825
Varsomers199472825
Maprs199472825
PheGenIrs199472825
hapmaprs199472825
1000 genomesrs199472825
hgdprs199472825
ensemblrs199472825
gopubmedrs199472825
geneviewrs199472825
scholarrs199472825
googlers199472825
pharmgkbrs199472825
gwascentralrs199472825
openSNPrs199472825
23andMers199472825
23andMe allrs199472825
SNP Nexus

SNPshotrs199472825
SNPdbers199472825
MSV3drs199472825
GWAS Ctlgrs199472825
Max Magnitude0
ClinVar
Risk rs199472825(C;C)
Alt rs199472825(C;C)
Reference rs199472825(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.150674955T>G
CLNSRC ClinVar
CLNACC RCV000058236.2,