rs7538876, PADI6

N. diseases: 6
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.
Basal Cell Cancer
CUI: C0751676
Disease: Basal Cell Cancer
109 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 3 2008 2015
Basal cell carcinoma
CUI: C0007117
Disease: Basal cell carcinoma
109 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 3 2008 2015
Basal Cell Neoplasm
CUI: C0206710
Disease: Basal Cell Neoplasm
109 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 3 2008 2015
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 2 2008 2014
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.700 1.000 1 2010 2010
melanoma
CUI: C0025202
Disease: melanoma
515 0.807 0.120 1 17395867 intron variant G/A snv 0.37 0.010 1.000 1 2013 2013