Variant (rsID / SNP)
rs1143679
rs1143679 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGAM. Location: chromosome 16, position 31,276,811. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 16:31276811
- HGVS
- NM_001145808.2,c.230G>A,p.Arg77His
- Allele change
- Missense_R77H
Associated conditions / phenotypes
Lupus Erythematosus|Systemic Lupus Erythematosus|Rheumatoid Arthritis|Autoimmune Disease|Arthritis|Scleroderma, Familial Progressive|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Exanthem|Celiac Disease 1|Juvenile Rheumatoid Arthritis|Peritonitis|Complement Deficiency|Systemic Lupus Erythematosus 6|Cutaneous Lupus Erythematosus|Discoid Lupus Erythematosus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.