DOK2, docking protein 2, 9046

N. diseases: 35; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34215892
rs34215892
Entrez Id: 9046
Gene Symbol: DOK2
DOK2
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs899428
rs899428
Entrez Id: 9046
Gene Symbol: DOK2
DOK2
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies. 31564439 2019
dbSNP: rs2242241
rs2242241
Entrez Id: 9046
Gene Symbol: DOK2
DOK2
CUI: C1832661
Disease:
ANOPHTHALMIA AND PULMONARY HYPOPLASIA 		0.010 GeneticVariation BEFREE We identify three low-frequency missense variants associated with the PDAC risk: rs34309238 in PKN1 (OR = 1.77, 95% CI: 1.48-2.12, P = 5.35 × 10<sup>-10</sup>), rs2242241 in DOK2 (OR = 1.85, 95% CI: 1.50-2.27, P = 4.34 × 10<sup>-9</sup>), and rs183117027 in APOB (OR = 2.34, 95% CI: 1.72-3.16, P = 4.21 × 10<sup>-8</sup>). 30206226 2018
dbSNP: rs2242241
rs2242241
Entrez Id: 9046
Gene Symbol: DOK2
DOK2
CUI: C2239176
Disease:
Liver carcinoma 		0.010 GeneticVariation BEFREE Seven polymorphisms of caspase 9 (rs2308941)C-->T and DOK2(rs2242241) T-->G, 6 of polymorphisms of EGFL3 (rs947345)A -->G, caspase 9 ( rs2308938) C-->G and PHGDH(rs1801955)T-->A, 5 of polymorphisms of E2F2(rs3218170) G-->A,4 of polymorphisms of MUTYH(rs1140507)T-->C and BNIP3L(rs1055806)G-->T, and 1 of polymorphism of TNFRSF1B (rs1061622)T-->G were detected by the chip in the tissues of 10 HCC. 16109524 2005