rs3116496, CD28

N. diseases: 11
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.030 1.000 3 2012 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.030 1.000 3 2012 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.030 1.000 3 2014 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.030 1.000 3 2014 2019
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2019 2019
leukemia
CUI: C0023418
Disease: leukemia
144 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2019 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1 2019 2019
Malignant neoplasm of colon and/or rectum
502 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2017 2017
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 0.010 1.000 1 2018 2018