Variant (rsID / SNP)
rs1053874
rs1053874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNASE1. Location: chromosome 16, position 3,707,747. Clinical significance in the table: risk factor.
Reference-table entries
DNASE1Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:3707747
- Cytoband
- 16p13.3
- HGVS
- NM_005223.4(DNASE1):c.731G>A (p.Arg244Gln)
- Allele change
- Missense_R244Q
Associated conditions / phenotypes
Systemic lupus erythematosus, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.