RS606231417 CTLA4
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
Inborn genetic diseases
Type 1 diabetes mellitus 12
Systemic lupus erythematosus
Celiac disease
susceptibility to
3
Hashimoto thyroiditis
Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency
Inborn genetic diseases
Type 1 diabetes mellitus 12
Systemic lupus erythematosus
Celiac disease
susceptibility to
3
Other Variants in CTLA4