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

rs17587

From SNPedia

Orientationplus
Stabilizedplus
Make rs17587(A;A)
Make rs17587(A;G)
Make rs17587(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32857313
GenePSMB9
is asnp
is mentioned by
dbSNPrs17587
ebirs17587
HLIrs17587
Exacrs17587
Varsomers17587
Maprs17587
PheGenIrs17587
hapmaprs17587
1000 genomesrs17587
hgdprs17587
ensemblrs17587
gopubmedrs17587
geneviewrs17587
scholarrs17587
googlers17587
pharmgkbrs17587
gwascentralrs17587
openSNPrs17587
23andMers17587
23andMe allrs17587
SNP Nexus

SNPshotrs17587
SNPdbers17587
MSV3drs17587
GWAS Ctlgrs17587
GMAF0.2231
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 22034108] Radiographic severity in ankylosing spondylitis is associated with polymorphism in large multifunctional peptidase 2 (LMP2) in the SPARCC cohort


[PMID 12830434OA-icon.png] BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.


GET Evidence
PSMB9-R60H
aa_change Arg60His
aa_change_short R60H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.230159
summary



[PMID 25528575OA-icon.png] Genetic variants in antigen presentation-related genes influence susceptibility to hepatitis C virus and viral clearance: a case control study