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: rs10119582
rs10119582
PTPRD
9 10060803 intron variant C/T snv 7.7E-02
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2018 2018
dbSNP: rs10759102
rs10759102
PTPRD
9 9910123 intron variant G/A snv 0.38
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.800 1.000 1 2012 2012
dbSNP: rs10958852
rs10958852
PTPRD
9 10060843 intron variant C/T snv 4.5E-04
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs10958852
rs10958852
PTPRD
9 10060843 intron variant C/T snv 4.5E-04
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs12003835
rs12003835
PTPRD
9 8424378 intron variant G/T snv 4.1E-02
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1322148
rs1322148
PTPRD
9 10251492 intron variant A/T snv 0.57
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs1323489
rs1323489
PTPRD
9 10369009 intron variant A/T snv 0.90
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1332813
rs1332813
PTPRD
9 9350706 intron variant T/C snv 0.63
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
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: 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: 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: 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: 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: 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: 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
dbSNP: rs620558
rs620558
PTPRD
9 10436921 intron variant A/G snv 0.16
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62529502
rs62529502
PTPRD
9 9142493 intron variant T/A snv 6.2E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs62529502
rs62529502
PTPRD
9 9142493 intron variant T/A snv 6.2E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs7865468
rs7865468
PTPRD
9 10274080 intron variant G/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2014 2014
dbSNP: rs10815925
rs10815925
PTPRD
0.925 0.120 9 8712601 intron variant C/G snv 0.41
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 1.000 1 2012 2012
dbSNP: rs10815925
rs10815925
PTPRD
0.925 0.120 9 8712601 intron variant C/G snv 0.41
CUI: C0018099
Disease: Gout
Gout 		0.700 1.000 1 2012 2012
dbSNP: rs17584499
rs17584499
PTPRD
0.925 0.080 9 8879118 intron variant C/T snv 0.14
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.820 1.000 1 2010 2016