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: rs4949718
rs4949718 		1 76433779 intron variant T/A;C snv
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.800 1.000 1 2013 2013
dbSNP: rs4949718
rs4949718 		1 76433779 intron variant T/A;C snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.800 1.000 1 2013 2013
dbSNP: rs10782606
rs10782606 		0.925 0.040 1 76215537 intron variant G/A snv 0.67
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10782606
rs10782606 		0.925 0.040 1 76215537 intron variant G/A snv 0.67
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2631781
rs2631781 		1.000 0.080 1 76128101 intron variant C/A;T snv
CUI: C3894553
Disease: response to simvastatin
response to simvastatin 		0.700 1.000 1 2018 2018
dbSNP: rs2631781
rs2631781 		1.000 0.080 1 76128101 intron variant C/A;T snv
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 2018 2018
dbSNP: rs4949718
rs4949718 		1 76433779 intron variant T/A;C snv
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2013 2013
dbSNP: rs915404
rs915404 		1 76136977 intron variant A/G snv 0.19
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.700 1.000 1 2010 2010
dbSNP: rs10873876
rs10873876 		1.000 0.040 1 76306643 intron variant T/C snv 0.75
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs12239582
rs12239582 		0.925 0.080 1 76371552 intron variant A/C snv 0.30
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12239582
rs12239582 		0.925 0.080 1 76371552 intron variant A/C snv 0.30
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018