Variant (rsID / SNP)
rs11203366
rs11203366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PADI4. Location: chromosome 1, position 17,657,534. Clinical significance in the table: association.
Reference-table entries
PADI4Association
- Clinical significance (as recorded)
- association
- Variant type
- missense_variant
- Chromosome / position
- 1:17657534
- HGVS
- NM_012387.3,c.163G>A,p.Gly55Ser
- Allele change
- Missense_G55S
Associated conditions / phenotypes
Rheumatoid Arthritis|Interstitial Lung Disease|Squamous Cell Carcinoma|Esophageal Cancer|Autoimmune Disease|Arthritis|Inflammatory Spondylopathy|Systemic Lupus Erythematosus|Spondyloarthropathy 1|Toxic Shock Syndrome|Spondylitis|Ulcerative Colitis|Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.