ATG16L1, autophagy related 16 like 1, 55054

N. diseases: 120; N. variants: 31
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2241880
rs2241880
Entrez Id: 55054;677775
Gene Symbol: ATG16L1;SCARNA5
ATG16L1;SCARNA5
CUI: C1623038
Disease:
Cirrhosis
0.010 GeneticVariation BEFREE The ATG16L1 gene variant rs2241880 (p.T300A) is associated with susceptibility to HCC in patients with cirrhosis. 31484215 2019