Variant (rsID / SNP)
rs2240340
rs2240340 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PADI4. Location: chromosome 1, position 17,662,639. Clinical significance in the table: association.
Reference-table entries
PADI4Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:17662639
- Cytoband
- 1p36.13
- HGVS
- NM_012387.3(PADI4):c.341-15T>C
- Allele change
- Silent
Associated conditions / phenotypes
Rheumatoid arthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.