Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs11574637

ITGAX

rs11574637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITGAX. Location: chromosome 16, position 31,368,874. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

ITGAXNot classified
Variant type
intron_variant
Chromosome / position
16:31368874
HGVS
NM_001286375.2,c.430+189T>C
Allele change
Silent

Associated conditions / phenotypes

Systemic Lupus Erythematosus|Autoimmune Disease|Lupus Erythematosus|Pemphigus Foliaceus|Systemic Lupus Erythematosus 12|Systemic Lupus Erythematosus 6|Scleroderma, Familial Progressive|Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity|Pemphigus

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.