rs4792311, ELAC2

N. diseases: 9
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.
PROSTATE CANCER, HEREDITARY, 2
CUI: C3539120
Disease: PROSTATE CANCER, HEREDITARY, 2
7 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.700 0
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.090 1.000 9 2002 2010
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.080 1.000 8 2002 2010
Prostate cancer, familial
CUI: C2931456
Disease: Prostate cancer, familial
25 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.030 0.667 3 2001 2010
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.020 1.000 2 2001 2001
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.010 1.000 1 2001 2001
Hereditary Prostate Carcinoma
CUI: C4722328
Disease: Hereditary Prostate Carcinoma
12 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.010 1.000 1 2001 2001
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.010 1.000 1 2016 2016
Pure Red-Cell Aplasia
CUI: C0034902
Disease: Pure Red-Cell Aplasia
7 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 0.010 1.000 1 2001 2001