Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6504108
rs6504108 		17 48215561 intron variant C/T snv 0.72
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2018
dbSNP: rs9303542
rs9303542 		0.882 0.120 17 48334138 intron variant A/G snv 0.34
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 2 2010 2013
dbSNP: rs9303542
rs9303542 		0.882 0.120 17 48334138 intron variant A/G snv 0.34
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 2 2010 2013
dbSNP: rs11079810
rs11079810 		17 48150484 intron variant C/T snv 0.16
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11079810
rs11079810 		17 48150484 intron variant C/T snv 0.16
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11079810
rs11079810 		17 48150484 intron variant C/T snv 0.16
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11079810
rs11079810 		17 48150484 intron variant C/T snv 0.16
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs113866544
rs113866544 		17 48193244 intron variant T/C snv 6.1E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs16954078
rs16954078 		17 48228765 intron variant T/A snv 0.14
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs16969990
rs16969990 		17 48153529 intron variant C/T snv 0.12
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs208015
rs208015 		17 48174984 intron variant T/C snv 0.94
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2278868
rs2278868 		0.925 0.080 17 48184809 missense variant C/T snv 4.0E-06; 0.63 0.55
CUI: C0014175
Disease: Endometriosis
Endometriosis 		Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs2278868
rs2278868 		0.925 0.080 17 48184809 missense variant C/T snv 4.0E-06; 0.63 0.55
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs7207826
rs7207826 		0.925 0.120 17 48423311 intron variant T/C snv 0.33
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7207826
rs7207826 		0.925 0.120 17 48423311 intron variant T/C snv 0.33
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs78428146
rs78428146 		17 48160646 intron variant A/G snv 1.3E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs8080031
rs8080031 		0.925 0.040 17 48262165 intron variant T/G snv 3.0E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs8080031
rs8080031 		0.925 0.040 17 48262165 intron variant T/G snv 3.0E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs882380
rs882380 		1.000 0.080 17 48216874 intron variant C/A snv 0.52
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs9303542
rs9303542 		0.882 0.120 17 48334138 intron variant A/G snv 0.34
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2015 2015