Variant (rsID / SNP)
rs17587
rs17587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSMB9. Location: chromosome 6, position 32,825,090. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 6:32825090
- HGVS
- NM_002800.5,c.179G>A,p.Arg60His
- Allele change
- Missense_R60H
Associated conditions / phenotypes
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1|Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6|Autoimmune Disease|Rheumatoid Arthritis|Cervical Cancer|Cervix Uteri Carcinoma in Situ|Cervical Intraepithelial Neoplasia|Inflammatory Spondylopathy|Hepatitis C|Spondyloarthropathy 1|Hepatitis C Virus|Spondylitis|Lung Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.