Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1762111
ABCA4
0.851 0.080 1 94021934 missense variant A/G snv 1.2E-03 1.3E-03 3
rs1800548
ABCA4
0.925 0.040 1 94077833 missense variant C/T snv 8.3E-04 8.9E-04 2
rs1800552
ABCA4
0.851 0.080 1 94010821 missense variant C/T snv 1.6E-03 1.5E-03 2
rs1801269
ABCA4
0.851 0.080 1 94041345 missense variant C/A;T snv 3.1E-04; 4.0E-06 2
rs28938473
ABCA4
0.882 0.040 1 94007731 missense variant G/A snv 3.0E-03 3.6E-03 2
rs61750200
ABCA4
0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 2
rs61750202
ABCA4
0.925 0.040 1 94055245 missense variant C/G;T snv 2.1E-04 2
rs61750639
ABCA4
0.882 0.080 1 94007710 missense variant C/T snv 8.0E-06 1.4E-05 2
rs61751374
ABCA4
0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 2
rs1800549
ABCA4
0.925 0.040 1 94030497 missense variant G/A snv 4.6E-03 1.6E-03 1
rs1800550
ABCA4
1.000 0.040 1 94025039 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs1800551
ABCA4
1.000 0.040 1 94021887 missense variant C/T snv 8.0E-06 1
rs1800553
ABCA4
0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 1
rs55732384
ABCA4
0.851 0.080 1 94111561 missense variant G/A snv 1.6E-05 2.1E-05 1
rs61748558
ABCA4
0.827 0.080 1 94063224 missense variant C/T snv 4.0E-06 7.0E-06 1
rs61749420
ABCA4
0.851 0.080 1 94060740 missense variant G/A snv 1.6E-05 7.0E-06 1
rs61750130
ABCA4
0.807 0.080 1 94031110 missense variant G/A snv 2.4E-04 2.3E-04 1
rs61750146
ABCA4
0.851 0.080 1 94029522 missense variant A/G snv 8.2E-06 7.0E-06 1
rs61750641
ABCA4
0.790 0.080 1 94005499 missense variant C/T snv 3.5E-04 4.7E-04 1
rs61751408
ABCA4
0.851 0.080 1 94005509 missense variant G/A snv 2.0E-04 1.7E-04 1