Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2096507
rs2096507
Entrez Id: 23181
Gene Symbol: DIP2A
DIP2A
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2070433
rs2070433
Entrez Id: 23181
Gene Symbol: DIP2A
DIP2A
CUI: C0200635
Disease:
Lymphocyte Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs16979358
rs16979358
Entrez Id: 23181
Gene Symbol: DIP2A
DIP2A
CUI: C0920296
Disease:
Developmental reading disorder 		0.010 GeneticVariation BEFREE However, we found no evidence of an association of SNP rs16979358 with DD. 26452339 2016
dbSNP: rs2255526
rs2255526
Entrez Id: 23181
Gene Symbol: DIP2A
DIP2A
CUI: C0920296
Disease:
Developmental reading disorder 		0.010 GeneticVariation BEFREE We observed a significantly increased DD risk associated with rs2255526 G allele (OR = 1.297, 95% CI = 1.036-1.623, Padjusted  = 0.023) and GG genotypes (OR = 1.833, 95% CI = 1.043-3.223, Padjusted  = 0.035), compared with their wild-type counterparts. 26452339 2016