Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934586
GML ; CYP11B1
0.827 0.200 8 142875012 missense variant C/T snv 2.4E-05 2.1E-05 5
rs387907572
CYP11B1 ; GML
0.851 0.240 8 142876278 missense variant G/A snv 7.0E-06 4
rs104894061
CYP11B1 ; GML
0.882 0.200 8 142876242 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 3
rs104894070
CYP11B1 ; GML
0.882 0.200 8 142879146 missense variant G/A;T snv 4.0E-06 3
rs104894071
CYP11B1 ; GML
0.882 0.200 8 142875730 missense variant G/T snv 3
rs104894143
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.882 0.240 10 102831535 missense variant A/G snv 7.0E-06 3
rs104894142
CYP17A1 ; CYP17A1-AS1 ; WBP1L
0.882 0.200 10 102832566 missense variant G/A snv 4.0E-06 1.4E-05 3
rs1296969984
GML ; CYP11B1
0.882 0.240 8 142876243 missense variant T/G snv 3
rs1221010438
CYP11B1 ; GML
0.925 0.200 8 142875013 missense variant G/A snv 4.0E-06 2
rs61754278
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.925 0.200 10 102832610 missense variant C/T snv 1.6E-05 1.4E-05 2
rs367833709
CYP17A1 ; WBP1L ; CYP17A1-AS1
0.925 0.200 10 102831525 missense variant G/A;C snv 4.0E-06; 1.2E-05 2
rs768260761
CYP2B6
0.925 0.200 19 41012795 missense variant C/A snv 4.0E-06 2
rs750428278
GML ; CYP11B1
0.925 0.200 8 142874419 missense variant A/G snv 4.0E-06 2
rs121913553
PLOD1
0.925 0.160 1 11970750 stop gained G/A;C snv 4.0E-06 2
rs763398879
WBP1L ; CYP17A1-AS1 ; CYP17A1
0.925 0.200 10 102830742 missense variant C/A;T snv 4.1E-06; 8.3E-06 2