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: 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: 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: 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: 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: rs2475335
rs2475335
PTPRD
0.882 0.080 9 10260263 intron variant C/A;T snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2018 2018
dbSNP: rs2475335
rs2475335
PTPRD
0.882 0.080 9 10260263 intron variant C/A;T snv
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.010 1.000 1 2018 2018
dbSNP: rs2475335
rs2475335
PTPRD
0.882 0.080 9 10260263 intron variant C/A;T snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2018 2018
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: 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: 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: 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: 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: rs649891
rs649891
PTPRD
1.000 0.080 9 10430602 intron variant T/A;C snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2016 2016
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: rs1335997
rs1335997
PTPRD
1.000 0.040 9 10467074 intron variant C/T snv 0.86
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: 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: 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: 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: 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: rs976831
rs976831
PTPRD
1.000 0.040 9 10479527 intron variant T/C snv 0.85
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs72700966
rs72700966
PTPRD
1.000 0.040 9 10505224 intron variant C/G;T snv
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.700 1.000 1 2014 2014
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