Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554776500
rs1554776500
SET
0.800 GeneticVariation UNIPROT De novo mutations in the SET nuclear proto-oncogene, encoding a component of the inhibitor of histone acetyltransferases (INHAT) complex in patients with nonsyndromic intellectual disability. 29688601

2018
dbSNP: rs1554776500
rs1554776500
SET
0.800 GeneticVariation UNIPROT De novo mutations in moderate or severe intellectual disability. 25356899

2014
dbSNP: rs1554776500
rs1554776500
SET
G 0.800 CausalMutation CLINVAR