rs2469696948
This variant is located in the ATG16L1 gene.
▶ClinVar annotation
About ATG16L1
The protein encoded by this gene is part of a large protein complex that is necessary for autophagy, the major process by which intracellular components are targeted to lysosomes for degradation. Defects in this gene are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]
View all ATG16L1 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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