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: rs35041767
rs35041767
PTPRD
1.000 0.080 9 9261737 intron variant -/C ins
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.700 1.000 1 2008 2008
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: 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: rs9644896
rs9644896
PTPRD
1.000 0.040 9 9334204 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: 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: 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: 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: 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: 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: 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: rs2053125
rs2053125
PTPRD
9 8831162 intron variant A/G snv 0.58
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
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: 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: 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: rs1332795
rs1332795
PTPRD
1.000 0.040 9 9338215 intron variant A/T snv 0.54
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: 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: 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: 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: rs58823963
rs58823963
PTPRD
1.000 0.040 9 9550389 intron variant C/A snv 0.23
CUI: C0877015
Disease: Pelvic Organ Prolapse
Pelvic Organ Prolapse 		0.700 1.000 1 2015 2015
dbSNP: rs138915427
rs138915427
PTPRD
1.000 0.080 9 8341723 missense variant C/A;G;T snv 4.0E-06; 2.0E-05; 2.4E-05
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.010 1.000 1 2011 2011
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: rs193407
rs193407
PTPRD
9 9059924 intron variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013