Variant (rsID / SNP)
rs763361
rs763361 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD226. Location: chromosome 18, position 67,531,642. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 18:67531642
- HGVS
- NM_001303618.2,c.919A>G,p.Ser307Gly
- Allele change
- Missense_S152G
Associated conditions / phenotypes
Autoimmune Disease|Rheumatoid Arthritis|Scleroderma, Familial Progressive|Multiple Sclerosis|Type 1 Diabetes Mellitus|Diabetes Mellitus|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Systemic Lupus Erythematosus|Lupus Erythematosus|Arthritis|Celiac Disease 1|Relapsing-Remitting Multiple Sclerosis|Vasculitis|Pulmonary Fibrosis|Demyelinating Disease|Neuromyelitis Optica|Polyendocrinopathy|Squamous Cell Carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.