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

rs731506

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs731506(G;G)
Make rs731506(G;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position150974896
GeneKCNH2
is asnp
is mentioned by
dbSNPrs731506
ebirs731506
HLIrs731506
Exacrs731506
Varsomers731506
Maprs731506
PheGenIrs731506
hapmaprs731506
1000 genomesrs731506
hgdprs731506
ensemblrs731506
gopubmedrs731506
geneviewrs731506
scholarrs731506
googlers731506
pharmgkbrs731506
gwascentralrs731506
openSNPrs731506
23andMers731506
23andMe allrs731506
SNP Nexus

SNPshotrs731506
SNPdbers731506
MSV3drs731506
GWAS Ctlgrs731506
Max Magnitude0
? (G;G) (G;T) (T;T) 28


ClinVar
Risk rs731506(C,G;C,G)
Alt rs731506(C,G;C,G)
Reference rs731506(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150671984A>G
CLNSRC ClinVar
CLNACC RCV000057876.2,