rs1447295, CASC8

N. diseases: 29
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 0.658 0.400 8 127472793 intron variant A/C;T snv 0.800 0.917 36 2007 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.658 0.400 8 127472793 intron variant A/C;T snv 0.800 0.914 35 2007 2019
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.658 0.400 8 127472793 intron variant A/C;T snv 0.700 1.000 1 2010 2010
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.658 0.400 8 127472793 intron variant A/C;T snv 0.040 1.000 4 2008 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.658 0.400 8 127472793 intron variant A/C;T snv 0.040 1.000 4 2008 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.658 0.400 8 127472793 intron variant A/C;T snv 0.030 1.000 3 2007 2014
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.658 0.400 8 127472793 intron variant A/C;T snv 0.020 1.000 2 2008 2014
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.658 0.400 8 127472793 intron variant A/C;T snv 0.020 0.500 2 2011 2013
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.658 0.400 8 127472793 intron variant A/C;T snv 0.020 1.000 2 2008 2014
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.658 0.400 8 127472793 intron variant A/C;T snv 0.020 1.000 2 2008 2014
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2012 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2008 2008
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2008 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1 2007 2007
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2007 2007
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2017 2017
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2008 2008
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1 2007 2007
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2017 2017
Malignant neoplasm of gastrointestinal tract
CUI: C0685938
Disease: Malignant neoplasm of gastrointestinal tract
55 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1 2017 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1.000 1 2012 2012
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1 2017 2017
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1 2012 2012
Primary differentiated carcinoma of thyroid gland
CUI: C4722172
Disease: Primary differentiated carcinoma of thyroid gland
41 0.658 0.400 8 127472793 intron variant A/C;T snv 0.010 1 2011 2011