Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs374657927
rs374657927
RIPK1 ; LOC107986556
A 0.700 CausalMutation CLINVAR Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases. 30591564

2019