Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs139271658
rs139271658
PTPRD
1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2019 2019
dbSNP: rs139271658
rs139271658
PTPRD
1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.700 1.000 1 2019 2019
dbSNP: rs1414557
rs1414557
PTPRD
1.000 0.040 9 10471937 intron variant C/A;G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs143575776
rs143575776
PTPRD
1.000 0.080 9 9593742 intron variant A/T snv 1.2E-02
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0.700 1.000 1 2017 2017
dbSNP: rs147345944
rs147345944
PTPRD
9 9479463 intron variant T/C;G snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs147345944
rs147345944
PTPRD
9 9479463 intron variant T/C;G snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs1475680
rs1475680
PTPRD
1.000 0.040 9 9405316 intron variant C/T snv 0.87
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1535459
rs1535459
PTPRD
1.000 0.080 9 10550204 intron variant C/G snv 1.1E-02
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.700 1.000 1 2016 2016
dbSNP: rs1547287
rs1547287
PTPRD
9 9354303 intron variant T/C snv 0.31
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs16926057
rs16926057
PTPRD
1.000 0.040 9 10467283 intron variant C/A snv 4.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17650729
rs17650729
PTPRD
9 8506459 intron variant C/G snv 2.6E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1836229
rs1836229
PTPRD
1.000 0.080 9 8820573 intron variant A/C;G;T snv
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.700 1.000 1 2017 2017
dbSNP: rs184140292
rs184140292
PTPRD
9 8457116 intron variant T/C snv 1.6E-03
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1865343
rs1865343
PTPRD
9 8845598 intron variant A/G snv 0.76
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1923357
rs1923357
PTPRD
1.000 0.080 9 10266786 intron variant C/T snv 0.72
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs1934268
rs1934268
PTPRD
9 9730366 intron variant C/T snv 0.86
CUI: C4280778
Disease: Modic type vertebral endplate changes
Modic type vertebral endplate changes 		0.700 1.000 1 2019 2019
dbSNP: rs1953595
rs1953595
PTPRD
1.000 0.040 9 10479485 intron variant A/T snv 0.70
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs201899638
rs201899638
PTPRD
9 9932324 intron variant T/C;G snv
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		0.700 1.000 1 2019 2019
dbSNP: rs2039332
rs2039332
PTPRD
1.000 0.080 9 9138642 intron variant C/T snv 0.10
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.700 1.000 1 2018 2018
dbSNP: rs2152510
rs2152510
PTPRD
1.000 0.040 9 10471487 intron variant C/T snv 0.88
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs2784598
rs2784598
PTPRD
0.925 0.040 9 10512307 intron variant T/A;C snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2784598
rs2784598
PTPRD
0.925 0.040 9 10512307 intron variant T/A;C snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs2784624
rs2784624
PTPRD
1.000 0.040 9 10478387 intron variant G/A snv 0.84
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs291269
rs291269
PTPRD
9 10043773 intron variant A/G snv 0.39
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2018 2018
dbSNP: rs35287509
rs35287509
PTPRD
9 10594635 intron variant T/C snv 0.26
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018