rs3789243, ABCB1

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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.030 1.000 3 2009 2013
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.020 1.000 2 2009 2013
Malignant neoplasm of colon and/or rectum
502 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.020 0.500 2 2009 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.020 1.000 2 2009 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.020 1.000 2 2009 2013
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1 2009 2009
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1 2009 2009
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1.000 1 2009 2009
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1.000 1 2016 2016
Idiopathic generalized epilepsy
CUI: C0270850
Disease: Idiopathic generalized epilepsy
24 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1.000 1 2009 2009
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1.000 1 2009 2009
Pancolitis
CUI: C0868908
Disease: Pancolitis
11 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1.000 1 2009 2009
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.120 7 87591570 intron variant A/G snv 0.50 0.010 1.000 1 2007 2007