DLG2, discs large MAGUK scaffold protein 2, 1740

N. diseases: 44; N. variants: 28
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: rs17148090
rs17148090 		11 85306432 intron variant A/C;G snv 7.4E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012
dbSNP: rs790356
rs790356 		1.000 0.160 11 83909744 intron variant A/G snv 0.50
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.800 1.000 1 2012 2012
dbSNP: rs1864774
rs1864774 		1.000 0.040 11 83488233 intron variant C/T snv 0.63
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2015 2019
dbSNP: rs349071
rs349071 		11 85065805 intron variant G/A snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs3793947
rs3793947 		1.000 0.040 11 83833429 intron variant G/A snv 0.42
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 2 2014 2017
dbSNP: rs10466716
rs10466716 		0.925 0.040 11 83654900 intron variant A/G snv 9.3E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10466716
rs10466716 		0.925 0.040 11 83654900 intron variant A/G snv 9.3E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1155311
rs1155311 		11 83778372 intron variant A/T snv 0.66
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs116875887
rs116875887 		11 85148382 intron variant C/A snv 1.2E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs117214796
rs117214796 		1.000 0.120 11 85160633 intron variant T/C snv 6.4E-03
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11823251
rs11823251 		11 85041870 intron variant C/G snv 0.23
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs142615018
rs142615018 		11 84759182 intron variant C/A;T snv 7.3E-03
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs150829342
rs150829342 		11 84107286 intron variant A/G snv 6.6E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs1532312
rs1532312 		11 85130529 intron variant C/T snv 0.32
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17807909
rs17807909 		1.000 0.080 11 84624623 intron variant T/G snv 1.1E-02
CUI: C2076600
Disease: Influenza due to Influenza A virus subtype H1N1
Influenza due to Influenza A virus subtype H1N1 		Infections; Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs189780858
rs189780858 		11 84206103 intron variant C/T snv 6.5E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs192772225
rs192772225 		11 84337159 intron variant G/A snv 3.9E-04
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs2155413
rs2155413 		1.000 0.040 11 84923746 intron variant C/A snv 0.55
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs286028
rs286028 		11 85394069 intron variant A/C;T snv
CUI: C0005910
Disease: Body Weight
Body Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2017 2017
dbSNP: rs286499
rs286499 		1.000 0.040 11 85482825 intron variant T/A;C;G snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2015 2015
dbSNP: rs349088
rs349088 		11 85103349 intron variant C/A snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs536665
rs536665 		11 85611356 intron variant A/G snv 0.13
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs655484
rs655484 		1.000 0.040 11 84472392 intron variant T/A;C snv
CUI: C0338480
Disease: Common Migraine
Common Migraine 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs74443493
rs74443493 		11 85186530 intron variant G/A snv 2.0E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7479949
rs7479949 		1.000 0.040 11 83792361 intron variant T/C snv 0.42
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2017 2017