Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs143609523
rs143609523
Entrez Id: 2589
Gene Symbol: GALNT1
GALNT1
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		G 0.700 GeneticVariation GWASCAT Identification of common genetic risk variants for autism spectrum disorder. 30804558 2019
dbSNP: rs16966921
rs16966921
Entrez Id: 2589
Gene Symbol: GALNT1
GALNT1
CUI: C0026470
Disease:
Monoclonal Gammopathy of Undetermined Significance 		0.010 GeneticVariation BEFREE Oncogene ALK and CDH2 were also identified to be moderately interacting with rs10251201 and rs16966921, two previously reported risk loci for MGUS. 30134812 2018