Source: ALL

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: rs10120450
rs10120450
PTPRD
9 8826588 intron variant T/C snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10120501
rs10120501
PTPRD
9 8826767 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10121203
rs10121203
PTPRD
9 8833227 intron variant A/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10511544
rs10511544
PTPRD
9 10319881 intron variant A/C snv 0.32
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2016 2016
dbSNP: rs10756026
rs10756026
PTPRD
9 10337976 intron variant T/A snv 0.34
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2016 2016
dbSNP: rs10758996
rs10758996
PTPRD
9 8827077 intron variant T/G snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
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: rs10809070
rs10809070
PTPRD
9 10341235 intron variant C/G snv 0.30
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		0.010 1.000 1 2016 2016
dbSNP: rs10815964
rs10815964
PTPRD
9 8826108 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
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: rs10977466
rs10977466
PTPRD
9 9065941 intron variant C/G;T snv 0.23
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
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: rs1331660
rs1331660
PTPRD
9 9039222 intron variant A/G snv 0.10
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.700 1.000 1 2011 2011
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: rs1337810
rs1337810
PTPRD
9 8610494 intron variant C/G snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1434254
rs1434254
PTPRD
9 8826278 intron variant C/T snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
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