Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs1141718
SOD2
0.724 0.280 6 159688224 missense variant A/G snv 15
rs4987023
SOD2
0.807 0.120 6 159692661 missense variant C/T snv 7.0E-06 6
rs5746136
SOD2
0.807 0.200 6 159682052 3 prime UTR variant C/T snv 0.27 6
rs781598341
SOD2
0.827 0.240 6 159682510 missense variant T/C snv 4.0E-06 5
rs6917589
SOD2
0.882 0.120 6 159678228 3 prime UTR variant T/C snv 0.22 3
rs11575993
SOD2
0.925 0.040 6 159688219 missense variant G/A snv 2
rs1165109290
SOD2
0.925 0.080 6 159692850 synonymous variant G/A snv 4.2E-06 2
rs1261281771
SOD2
0.925 0.080 6 159688191 missense variant C/G snv 7.0E-06 2
rs2758330
SOD2
0.925 0.080 6 159683812 intron variant G/T snv 0.77 2
rs2758331
SOD2
0.925 0.080 6 159684038 intron variant C/A snv 0.40 2
rs2758339
SOD2
0.925 0.080 6 159691552 3 prime UTR variant A/C;T snv 2
rs2842958
SOD2
0.925 0.080 6 159687393 intron variant A/G snv 0.77 2
rs370671213
SOD2
0.925 0.080 6 159692722 missense variant G/A;C snv 8.0E-06; 4.0E-06 2
rs748423903
SOD2
0.925 0.080 6 159688144 missense variant C/G;T snv 8.0E-06 2
rs779731636
SOD2
0.925 0.120 6 159685026 missense variant C/A snv 8.6E-06 2
rs1019827482
SOD2
1.000 6 159692550 missense variant T/C snv 6.0E-06 1
rs1176281575
SOD2
1.000 0.040 6 159684905 missense variant G/A snv 4.0E-06 1
rs1264525329
SOD2
1.000 0.120 6 159682587 missense variant T/C snv 4.0E-06 1
rs1336268032
SOD2
1.000 0.040 6 159692718 missense variant C/T snv 7.0E-06 1
rs1799725
SOD2
6 159692840 missense variant A/G snv 1
rs2842980
SOD2
1.000 0.040 6 159679084 3 prime UTR variant A/T snv 0.77 1
rs4342445
SOD2
6 159677190 3 prime UTR variant G/A snv 0.22 1
rs5746098
SOD2
1.000 0.080 6 159692589 missense variant T/C snv 9.6E-05 1.4E-05 1