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: 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: rs137852578
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.020 1.000 2 2002 2012
dbSNP: rs1057519864
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 1.000 1 2017 2017
dbSNP: rs1057519912
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms 		0.010 < 0.001 1 2013 2013
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
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