DOK5, docking protein 5, 55816

N. diseases: 11; N. variants: 8
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2023454
rs2023454 		1.000 0.040 20 54650572 3 prime UTR variant C/G snv 0.13
CUI: C0376335
Disease: fMRI
fMRI 		0.700 1.000 1 2010 2010
dbSNP: rs2023454
rs2023454 		1.000 0.040 20 54650572 3 prime UTR variant C/G snv 0.13
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2841
rs2841 		1.000 0.040 20 54651054 3 prime UTR variant G/A snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2904388
rs2904388 		1.000 0.040 20 54650158 intron variant T/C snv 0.70
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6023383
rs6023383 		0.925 0.040 20 54586887 intron variant C/T snv 0.14
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6023383
rs6023383 		0.925 0.040 20 54586887 intron variant C/T snv 0.14
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs6068930
rs6068930 		1.000 0.040 20 54650267 intron variant A/G snv 1.0E-01
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6064099
rs6064099 		0.925 0.120 20 54643425 intron variant G/C snv 0.30 0.36
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs6064099
rs6064099 		0.925 0.120 20 54643425 intron variant G/C snv 0.30 0.36
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs6068916
rs6068916 		1.000 0.080 20 54616992 intron variant T/A;C;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs873079
rs873079 		1.000 0.080 20 54643947 intron variant G/A snv 0.30
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2010 2010