Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912446
SCAF4 ; SOD1
1.000 0.080 21 31668547 missense variant T/C snv 1
rs121912451
SCAF4 ; SOD1
0.925 0.080 21 31668517 missense variant G/A;C snv 4.0E-06 1
rs1424014997
SCAF4 ; SOD1
0.882 0.080 21 31668562 missense variant T/C snv 8.0E-06 1
rs1476760624
SCAF4 ; SOD1
1.000 0.080 21 31668559 missense variant T/G snv 4.0E-06 1
rs11556620
SOD1
1.000 0.080 21 31667278 missense variant A/G;T snv 1
rs121912431
SOD1
0.742 0.160 21 31663829 missense variant G/A;C snv 1
rs121912432
SOD1
0.925 0.080 21 31663832 missense variant C/G snv 4.0E-06 1
rs121912433
SOD1
0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 1
rs121912434
SOD1
0.925 0.080 21 31663842 missense variant G/A snv 1
rs121912435
SOD1
0.925 0.080 21 31663848 missense variant A/G snv 4.0E-06 1
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 1
rs121912437
SOD1
0.851 0.080 21 31667298 missense variant G/A;C;T snv 1
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 1
rs121912439
SOD1
0.851 0.080 21 31667320 missense variant A/G snv 1
rs121912440
SOD1
0.882 0.080 21 31667337 missense variant C/G;T snv 1
rs121912441
SOD1
0.925 0.080 21 31667359 missense variant T/C snv 4.8E-05 7.0E-06 1
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 1
rs121912445
SOD1
0.882 0.080 21 31667331 missense variant A/T snv 1
rs121912452
SOD1
0.807 0.120 21 31667271 missense variant T/C;G snv 4.0E-06 1
rs121912455
SOD1
0.882 0.080 21 31666496 missense variant G/A;T snv 4.0E-06 1
rs121912457
SOD1
1.000 0.080 21 31663854 missense variant T/C;G snv 1
rs1235629842
SOD1
1.000 0.080 21 31667373 missense variant G/C;T snv 4.0E-06 1
rs1280042397
SOD1
1.000 0.080 21 31667287 missense variant C/T snv 1.2E-05 7.0E-06 1
rs1301635320
SOD1
1.000 0.080 21 31667364 missense variant C/G;T snv 8.0E-06; 4.0E-06 1
rs1315541036
SOD1
0.925 0.080 21 31667273 missense variant G/A;C snv 4.0E-06; 4.0E-06 1