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: 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 5 2010 2016
dbSNP: rs4626664
rs4626664
PTPRD
1.000 0.080 9 9261737 intron variant G/A snv 0.20
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.820 1.000 3 2008 2014
dbSNP: rs1975197
rs1975197
PTPRD
1.000 0.080 9 8846955 intron variant G/A snv 0.16
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.810 1.000 3 2008 2011
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: rs10118330
rs10118330
PTPRD
1.000 0.040 9 9404090 intron variant A/G snv 3.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: rs10122096
rs10122096
PTPRD
1.000 0.040 9 9405431 intron variant G/A snv 0.87
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: rs10759062
rs10759062
PTPRD
1.000 0.040 9 9404584 intron variant T/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10759063
rs10759063
PTPRD
1.000 0.040 9 9404813 intron variant G/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs10759064
rs10759064
PTPRD
1.000 0.040 9 9405003 intron variant A/G snv 0.55
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: 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: rs10816124
rs10816124
PTPRD
1.000 0.040 9 9404896 intron variant C/A snv 7.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: rs10978121
rs10978121
PTPRD
1.000 0.040 9 9945648 intron variant T/C snv 8.7E-02
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia 		0.700 1.000 1 2011 2011
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: rs1322281
rs1322281
PTPRD
1.000 0.040 9 10582445 intron variant T/C snv 0.76
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2016 2016