Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29 8
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519922
NFE2L2
0.790 0.200 2 177234082 missense variant C/G;T snv 7
rs1057519923
NFE2L2
0.807 0.200 2 177234081 missense variant T/A snv 6
rs1057519924
NFE2L2
0.807 0.200 2 177234080 missense variant C/A snv 6
rs6726395
NFE2L2
0.851 0.240 2 177238501 intron variant A/G snv 0.52 4
rs750553272
NFE2L2
0.851 0.080 2 177230898 missense variant G/A snv 1.2E-05 7.0E-06 4
rs746497256
NFE2L2
0.925 0.080 2 177231925 synonymous variant A/G snv 8.0E-06 7.0E-06 3
rs1553488015
NFE2L2
0.925 0.080 2 177234226 missense variant C/T snv 2
rs587778556
NFE2L2
2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 2
rs755135182
NFE2L2
2 177231657 missense variant G/A snv 4.0E-06 2
rs767964519
NFE2L2
0.925 0.120 2 177231869 missense variant T/C snv 4.0E-06 2
rs12471433
MIR3128 ; NFE2L2
2 177257637 intron variant A/C snv 0.29 1
rs10497511
NFE2L2
1.000 0.080 2 177254568 intron variant G/A;C snv 1
rs1185894299
NFE2L2
1.000 0.040 2 177232545 synonymous variant A/T snv 4.0E-06 7.0E-06 1
rs1434704960
NFE2L2
1.000 0.080 2 177231543 missense variant C/T snv 1
rs1469602964
NFE2L2
1.000 0.040 2 177233301 missense variant A/T snv 4.1E-06 1
rs1553487942
NFE2L2
1.000 2 177234076 missense variant C/T snv 1
rs1553487947
NFE2L2
1.000 2 177234078 missense variant G/T snv 1
rs17581525
NFE2L2
2 177281634 intron variant C/G snv 0.26 1
rs1806649
NFE2L2
1.000 0.040 2 177253424 intron variant C/T snv 0.17 1
rs1962142
NFE2L2
1.000 0.080 2 177248756 intron variant A/G;T snv 1
rs2364723
NFE2L2
1.000 0.080 2 177261818 intron variant G/A;C;T snv 1