Variant (rsID / SNP)
rs2277798
rs2277798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBASH3A. Location: chromosome 21, position 43,824,106. The table records no clinical significance for this variant.
Reference-table entries
UBASH3ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 21:43824106
- HGVS
- NM_018961.4,c.52A>G,p.Ser18Gly
- Allele change
- Missense_S18G
Associated conditions / phenotypes
Autoimmune Disease|Systemic Lupus Erythematosus|Lupus Erythematosus|Exanthem|Aphthous Stomatitis|Vasculitis|Rheumatoid Arthritis|Arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.