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
rs387907201
F2
1.000 0.080 11 46739326 missense variant G/A;T snv 4
rs1176447366
TINAGL1
0.882 0.080 1 31586845 missense variant G/A snv 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
rs143498218
F2
0.925 0.080 11 46728732 missense variant G/A;C snv 2.4E-05; 8.0E-06 2
rs121918483
F2
1.000 0.080 11 46726734 missense variant G/A snv 4.9E-04 1
rs121918484
F2
1.000 0.080 11 46726761 missense variant G/A snv 4.0E-06 1.4E-05 1
rs121918485
F2
1.000 0.080 11 46728139 missense variant G/A snv 4.1E-06 1
rs121918486
F2
1.000 0.080 11 46739324 missense variant C/G snv 1
rs1361766713
F2
1.000 0.080 11 46729505 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 8.0E-06 1