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: rs12633551
rs12633551 		3 12318995 intron variant C/T snv 2.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs13061415
rs13061415 		1.000 0.040 3 12308425 intron variant T/C snv 0.28
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs13064760
rs13064760 		3 12327902 intron variant C/T snv 8.8E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs13064760
rs13064760 		3 12327902 intron variant C/T snv 8.8E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs13306745
rs13306745 		3 12379557 intron variant G/T snv 3.3E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13306745
rs13306745 		3 12379557 intron variant G/T snv 3.3E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17036160
rs17036160 		1.000 0.080 3 12288284 intron variant C/T snv 8.8E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17036170
rs17036170 		1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		Digestive System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2012 2012
dbSNP: rs17036170
rs17036170 		1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease 		Digestive System Diseases; Chemically-Induced Disorders 0.700 1.000 1 2012 2012
dbSNP: rs17036188
rs17036188 		0.882 0.120 3 12299426 intron variant T/C snv 4.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17036321
rs17036321 		3 12343100 intron variant T/C;G snv 2.5E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17036321
rs17036321 		3 12343100 intron variant T/C;G snv 2.5E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17036326
rs17036326 		1.000 0.040 3 12347814 intron variant A/G snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17036328
rs17036328 		1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17036328
rs17036328 		1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17036328
rs17036328 		1.000 0.040 3 12348985 intron variant T/C snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs17793693
rs17793693 		1.000 0.040 3 12304472 intron variant C/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1797912
rs1797912 		1.000 0.040 3 12428740 intron variant A/C snv 0.33
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1797912
rs1797912 		1.000 0.040 3 12428740 intron variant A/C snv 0.33
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1801282
rs1801282 		0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2012 2012
dbSNP: rs1801282
rs1801282 		0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs1801282
rs1801282 		0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1899951
rs1899951 		0.851 0.160 3 12353341 intron variant C/T snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs2960422
rs2960422 		1.000 0.080 3 12293492 intron variant G/A snv 0.59
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs35240997
rs35240997 		3 12337852 intron variant A/G snv 0.20
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019