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.
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
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2012 2012
Primary differentiated carcinoma of thyroid gland
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
41 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2012 2012
Pseudohyperkalemia Cardiff
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
60 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2016 2016
Rickets
CUI: C0035579
Disease: Rickets
16 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2013 2013
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
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