Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs976306779
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2008 2008
dbSNP: rs1571801
rs1571801
DAB2IP
0.827 0.120 9 121665094 intron variant G/T snv 0.21
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2007 2007
dbSNP: rs28909982
rs28909982
CHEK2
0.925 0.080 22 28725338 missense variant T/C snv 1.2E-04 9.1E-05
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2006 2006
dbSNP: rs587782480
rs587782480
CHEK2
22 28699888 missense variant T/C snv 4.0E-06
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2006 2006
dbSNP: rs786202601
rs786202601
CHEK2
1.000 0.120 22 28694059 frameshift variant T/- delins
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2006 2006
dbSNP: rs137852581
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2004 2004