rs10741657, CYP2R1

N. diseases: 34
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.820 1.000 3 2010 2018
Vitamin D measurement
CUI: C0919758
Disease: Vitamin D measurement
51 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.700 1.000 1 2018 2018
Vitamin D3 measurement
CUI: C0523979
Disease: Vitamin D3 measurement
51 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.700 1.000 1 2018 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.020 1.000 2 2014 2015
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.020 1.000 2 2013 2019
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2015 2015
Chlamydia Infections
CUI: C0008149
Disease: Chlamydia Infections
10 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2016 2016
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2012 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2014 2014
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2018 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2018 2018
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1 2007 2007
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2018 2018
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2012 2012
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2018 2018
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2012 2012
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2019 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2018 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2011 2011