rs587777627, POLD1

N. diseases: 7
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.
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.807 0.080 19 50406444 missense variant T/C snv 0.800 1.000 4 2006 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.807 0.080 19 50406444 missense variant T/C snv 0.700 1.000 4 2006 2017
Adult Oligodendroglioma
CUI: C0279070
Disease: Adult Oligodendroglioma
19 0.807 0.080 19 50406444 missense variant T/C snv 0.010 1.000 1 2016 2016
Childhood Oligodendroglioma
CUI: C0280475
Disease: Childhood Oligodendroglioma
19 0.807 0.080 19 50406444 missense variant T/C snv 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.807 0.080 19 50406444 missense variant T/C snv 0.010 1.000 1 2016 2016
oligodendroglioma
CUI: C0028945
Disease: oligodendroglioma
21 0.807 0.080 19 50406444 missense variant T/C snv 0.010 1.000 1 2016 2016
Well Differentiated Oligodendroglioma
22 0.807 0.080 19 50406444 missense variant T/C snv 0.010 1.000 1 2016 2016