Variant (rsID / SNP)
rs11755393
rs11755393 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UHRF1BP1. Location: chromosome 6, position 34,824,636. The table records no clinical significance for this variant.
Reference-table entries
UHRF1BP1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:34824636
- HGVS
- NM_017754.4,c.1361A>G,p.Gln454Arg
- Allele change
- Missense_Q454R
Associated conditions / phenotypes
Systemic Lupus Erythematosus|Autoimmune Disease|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.