Disease: Immunoglobulin A deficiency (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16862780
rs16862780
Entrez Id: 105374266
Gene Symbol: LINC01991
LINC01991
CUI: C0162538
Disease:
Immunoglobulin A deficiency (disorder) 		0.700 GeneticVariation GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758 2016