rs386675647, UGT2B7

N. diseases: 10
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.
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.020 1.000 2 2005 2008
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.020 1.000 2 2005 2008
Malignant neoplasm of urinary bladder
316 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.020 1.000 2 2005 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2011 2011
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2009 2009
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2011 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2002 2002
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2004 2004
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.790 0.240 4 69098619 missense variant AT/TC mnv 0.010 1.000 1 2002 2002