rs744154, ERCC4

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.
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.020 1.000 2 2013 2013
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.020 1.000 2 2013 2013
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2010 2010
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2006 2006
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2010 2010
Invasive carcinoma of breast
CUI: C0853879
Disease: Invasive carcinoma of breast
21 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2009 2009
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2006 2006
Malignant neoplasm of urinary bladder
316 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2010 2010
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1 2012 2012
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1 2012 2012
Xeroderma pigmentosum, group F
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
31 0.763 0.280 16 13921224 intron variant G/C snv 0.23 0.010 1.000 1 2010 2010