rs3803185, ARL11

N. diseases: 19
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 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.040 0.750 4 2006 2011
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.030 1.000 3 2006 2006
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.030 1.000 3 2008 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.030 1.000 3 2007 2017
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.030 1.000 3 2008 2013
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.020 1.000 2 2006 2007
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.020 1.000 2 2007 2008
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.020 1.000 2 2007 2017
Prostate cancer, familial
CUI: C2931456
Disease: Prostate cancer, familial
25 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.020 1.000 2 2008 2011
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2011 2011
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2006 2006
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2009 2009
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2006 2006
Hereditary Malignant Neoplasm
CUI: C1333600
Disease: Hereditary Malignant Neoplasm
18 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2017 2017
Hereditary Prostate Carcinoma
CUI: C4722328
Disease: Hereditary Prostate Carcinoma
12 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2011 2011
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2009 2009
melanoma
CUI: C0025202
Disease: melanoma
515 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2006 2006
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2006 2006
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2009 2009