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.
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, 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
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
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
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
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
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2019 2019
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2019 2019