Variant (rsID / SNP)
rs2240335
rs2240335 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PADI4. Location: chromosome 1, position 17,674,537. The table records no clinical significance for this variant.
Reference-table entries
PADI4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:17674537
- HGVS
- NM_012387.3,c.1149C>A,p.Arg383Arg
- Allele change
- Synonymous_R383R
Associated conditions / phenotypes
Rheumatoid Arthritis|Arthritis|Iga Glomerulonephritis|Lateral Sclerosis|Amyotrophic Lateral Sclerosis 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.