rs486907, RNASEL

N. diseases: 32
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, SUSCEPTIBILITY TO
CUI: C3469524
Disease: PROSTATE CANCER, SUSCEPTIBILITY TO
6 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.700 0
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.100 0.708 24 2002 2019
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.100 0.708 24 2002 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.060 1.000 6 2004 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.050 1.000 5 2004 2019
Prostate cancer, familial
CUI: C2931456
Disease: Prostate cancer, familial
25 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.030 1.000 3 2004 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.020 1.000 2 2005 2007
Hereditary pancreatitis
CUI: C0238339
Disease: Hereditary pancreatitis
108 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.020 1.000 2 2002 2004
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.020 1.000 2 2005 2007
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.020 1.000 2 2008 2015
Prostatic Neoplasms
CUI: C0033578
Disease: Prostatic Neoplasms
31 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.020 1.000 2 2006 2009
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1 2004 2004
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2005 2005
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2008 2008
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2011 2011
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2011 2011
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2017 2017
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2007 2007
Hereditary Prostate Carcinoma
CUI: C4722328
Disease: Hereditary Prostate Carcinoma
12 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2004 2004
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2007 2007
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1 2004 2004
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1 2005 2005
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2011 2011
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1.000 1 2005 2005
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 0.010 1 2005 2005