Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs373562040
rs373562040
SLC39A8
0.700 GeneticVariation UNIPROT SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation. 26637979

2015
dbSNP: rs373562040
rs373562040
SLC39A8
0.700 GeneticVariation UNIPROT Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. 26637978

2015