Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs757240974
F2
0.851 0.080 11 46728060 missense variant C/T snv 4.1E-06 4
rs770671957
F10
0.882 0.080 13 113149326 missense variant C/G;T snv 8.0E-06; 4.0E-06 3
rs781413602
F10
0.882 0.080 13 113149087 missense variant G/A;T snv 1.6E-05; 4.0E-06 3
rs121918477
F2
0.925 0.080 11 46726563 missense variant C/T snv 4.0E-06 2
rs121918478
F2
0.925 0.080 11 46728746 missense variant C/T snv 8.0E-06 7.0E-06 2
rs121918479
F2
0.925 0.080 11 46728138 missense variant C/T snv 2
rs121918480
F2
0.925 0.080 11 46739341 missense variant G/T snv 2
rs121918481
F2
0.925 0.080 11 46728004 missense variant T/C snv 2
rs121918482
F2
1.000 0.080 11 46728157 missense variant G/A snv 2
rs62623459
F2
1.000 0.080 11 46725897 missense variant G/A snv 1.1E-03 1.4E-03 2
rs387906522
F2
1.000 0.080 11 46723421 frameshift variant -/T ins 4.0E-06 1
rs754231232
F2
1.000 0.080 11 46726564 missense variant G/A snv 4.0E-06 1