UNC5D, unc-5 netrin receptor D, 137970

N. diseases: 24; N. variants: 5
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: rs13280010
rs13280010 		8 35406221 intron variant C/T snv 0.33
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1528706
rs1528706 		0.925 0.040 8 35242247 intron variant C/T snv 0.12
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1528706
rs1528706 		0.925 0.040 8 35242247 intron variant C/T snv 0.12
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs16875831
rs16875831 		1.000 0.080 8 35396116 intron variant A/G snv 2.5E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C4722277
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 2
NEUROPATHY, CONGENITAL HYPOMYELINATING, 2 		0.700 1.000 1 2017 2017
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C0206172
Disease: Diabetic Foot
Diabetic Foot 		Skin and Connective Tissue Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C0154754
Disease: Hereditary and idiopathic neuropathy, unspecified
Hereditary and idiopathic neuropathy, unspecified 		Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C0442874
Disease: Neuropathy
Neuropathy 		Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28485846
rs28485846 		0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02
CUI: C4748608
Disease: NEUROPATHY, CONGENITAL HYPOMYELINATING, 3
NEUROPATHY, CONGENITAL HYPOMYELINATING, 3 		0.700 1.000 1 2017 2017
dbSNP: rs6468316
rs6468316 		8 35380270 intron variant C/T snv 0.53
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018