Have questions? Visit https://www.reddit.com/r/SNPedia

rs199472865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199472865(C;C)
Make rs199472865(C;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150959598
GeneKCNH2
is asnp
is mentioned by
dbSNPrs199472865
ebirs199472865
HLIrs199472865
Exacrs199472865
Varsomers199472865
Maprs199472865
PheGenIrs199472865
hapmaprs199472865
1000 genomesrs199472865
hgdprs199472865
ensemblrs199472865
gopubmedrs199472865
geneviewrs199472865
scholarrs199472865
googlers199472865
pharmgkbrs199472865
gwascentralrs199472865
openSNPrs199472865
23andMers199472865
23andMe allrs199472865
SNP Nexus

SNPshotrs199472865
SNPdbers199472865
MSV3drs199472865
GWAS Ctlgrs199472865
Max Magnitude0
ClinVar
Risk rs199472865(C,T;C,T)
Alt rs199472865(C,T;C,T)
Reference rs199472865(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.150656686C>G
CLNSRC ClinVar
CLNACC RCV000058235.2,