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

rs794729053

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729053(C;C)
Make rs794729053(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position41767470
GeneJUP
is asnp
is mentioned by
dbSNPrs794729053
ebirs794729053
HLIrs794729053
Exacrs794729053
Varsomers794729053
Maprs794729053
PheGenIrs794729053
hapmaprs794729053
1000 genomesrs794729053
hgdprs794729053
ensemblrs794729053
gopubmedrs794729053
geneviewrs794729053
scholarrs794729053
googlers794729053
pharmgkbrs794729053
gwascentralrs794729053
openSNPrs794729053
23andMers794729053
23andMe allrs794729053
SNP Nexus

SNPshotrs794729053
SNPdbers794729053
MSV3drs794729053
GWAS Ctlgrs794729053
Max Magnitude0
ClinVar
Risk rs794729053(C;C)
Alt rs794729053(C;C)
Reference rs794729053(T;T)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia
Variation info
Gene JUP
CLNDBN Cardiac arrhythmia
Reversed 1
HGVS NC_000017.10:g.39923722A>G
CLNSRC
CLNACC RCV000183509.1,