rs2745557, PACERR;PTGS2

N. diseases: 6
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.
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.807 0.200 1 186680089 intron variant A/G snv 0.83 0.030 1.000 3 2007 2016
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.807 0.200 1 186680089 intron variant A/G snv 0.83 0.030 1.000 3 2007 2016
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.807 0.200 1 186680089 intron variant A/G snv 0.83 0.010 1.000 1 2008 2008
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.807 0.200 1 186680089 intron variant A/G snv 0.83 0.010 1.000 1 2016 2016
Obesity
CUI: C0028754
Disease: Obesity
1111 0.807 0.200 1 186680089 intron variant A/G snv 0.83 0.010 1.000 1 2016 2016
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.807 0.200 1 186680089 intron variant A/G snv 0.83 0.010 1 2009 2009