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: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		0.820 1.000 3 2010 2018
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.020 1.000 2 2014 2015
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.020 1.000 2 2013 2019
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2014 2014
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2014 2014
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0011847
Disease: Diabetes
Diabetes 		0.010 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
Primary differentiated carcinoma of thyroid gland 		0.010 1.000 1 2012 2012
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0035579
Disease: Rickets
Rickets 		0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0008149
Disease: Chlamydia Infections
Chlamydia Infections 		0.010 1.000 1 2016 2016
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia 		0.010 1.000 1 2015 2015
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2019 2019
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.010 1.000 1 2019 2019
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0206682
Disease: Follicular thyroid carcinoma
Follicular thyroid carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2013 2013
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		0.010 1.000 1 2015 2015
dbSNP: rs10741657
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.010 1.000 1 2013 2013