Variant (rsID / SNP)
rs7574865
rs7574865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STAT4. Location: chromosome 2, position 191,964,633. Clinical significance in the table: risk factor.
Reference-table entries
STAT4Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:191964633
- Cytoband
- 2q32.2
- HGVS
- NM_003151.4(STAT4):c.274-23582=
- Allele change
- Silent
Associated conditions / phenotypes
Systemic lupus erythematosus, susceptibility to, 11
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.