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rs794728380

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728380(C;C)
Make rs794728380(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951442
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728380
ebirs794728380
HLIrs794728380
Exacrs794728380
Varsomers794728380
Maprs794728380
PheGenIrs794728380
hapmaprs794728380
1000 genomesrs794728380
hgdprs794728380
ensemblrs794728380
gopubmedrs794728380
geneviewrs794728380
scholarrs794728380
googlers794728380
pharmgkbrs794728380
gwascentralrs794728380
openSNPrs794728380
23andMers794728380
23andMe allrs794728380
SNP Nexus

SNPshotrs794728380
SNPdbers794728380
MSV3drs794728380
GWAS Ctlgrs794728380
Max Magnitude0
ClinVar
Risk rs794728380(C;C)
Alt rs794728380(C;C)
Reference rs794728380(T;T)
Significance Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene KCNH2
CLNDBN not provided Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648530A>G
CLNSRC
CLNACC RCV000181831.2, RCV000227185.1,