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rs770047651

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770047651(C;T)
Make rs770047651(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position150957291
GeneKCNH2
is asnp
is mentioned by
dbSNPrs770047651
ebirs770047651
HLIrs770047651
Exacrs770047651
Varsomers770047651
Maprs770047651
PheGenIrs770047651
hapmaprs770047651
1000 genomesrs770047651
hgdprs770047651
ensemblrs770047651
gopubmedrs770047651
geneviewrs770047651
scholarrs770047651
googlers770047651
pharmgkbrs770047651
gwascentralrs770047651
openSNPrs770047651
23andMers770047651
23andMe allrs770047651
SNP Nexus

SNPshotrs770047651
SNPdbers770047651
MSV3drs770047651
GWAS Ctlgrs770047651
Max Magnitude0
ClinVar
Risk rs770047651(T;T)
Alt rs770047651(T;T)
Reference rs770047651(C;C)
Significance Probable-Pathogenic
Disease Long QT syndrome not provided
Variation info
Gene KCNH2
CLNDBN Long QT syndrome not provided
Reversed 0
HGVS NC_000007.13:g.150654379C>T
CLNSRC
CLNACC RCV000200566.2, RCV000223833.1,