Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs5746105
SOD2
1.000 0.080 6 159691606 3 prime UTR variant A/G snv 0.28 1
rs5746134
SOD2
6 159682083 3 prime UTR variant G/A;C snv 1
rs6912979
SOD2
6 159699767 intron variant T/C snv 0.27 1
rs751648572
SOD2
1.000 0.080 6 159682631 missense variant A/C snv 4.1E-06 1
rs777153938
SOD2
1.000 0.080 6 159692615 missense variant T/G snv 1
rs8031
SOD2
1.000 0.040 6 159679608 3 prime UTR variant A/T snv 0.43 1
rs1419367513
SOD2 ; ACAT2 ; SOD2-OT1
6 159762678 non coding transcript exon variant G/A snv 1
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