rs4646536, CYP27B1

N. diseases: 14
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.
Abnormal renal morphology
CUI: C4551596
Disease: Abnormal renal morphology
3 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2019 2019
Asthma
CUI: C0004096
Disease: Asthma
1536 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2017 2017
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2015 2015
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2013 2013
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2017 2017
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2017 2017
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2013 2013
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2012 2012
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
28 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2012 2012
Lichen Planus, Oral
CUI: C0206139
Disease: Lichen Planus, Oral
20 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2012 2012
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2012 2012
Primary differentiated carcinoma of thyroid gland
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
41 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2012 2012
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 0.010 1.000 1 2019 2019