Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1223231582
PRSS1
0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1557055405
ABCD1
0.807 0.400 X 153743532 missense variant T/A snv 21
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29 8
rs1557055311
ABCD1
0.882 0.200 X 153743220 splice acceptor variant G/A;C snv 5
rs1569540688
ABCD1 ; BCAP31
0.925 0.240 X 153725586 missense variant T/C snv 4
rs26907
RASGRF2
0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs398123108
ABCD1
0.925 0.200 X 153743211 intron variant G/A;T snv 3
rs128624223
ABCD1
0.925 0.160 X 153740147 missense variant C/T snv 2
rs128624225
ABCD1
0.925 0.160 X 153743023 missense variant C/T snv 9.4E-06 2
rs864309520
BCAP31 ; ABCD1
1.000 0.160 X 153725917 missense variant G/C snv 2
rs973742 0.925 0.160 1 158190738 downstream gene variant G/A snv 0.42 2
rs1057517954
ABCD1 ; BCAP31
1.000 0.160 X 153725754 missense variant G/A snv 1
rs1064793877
ABCD1
1.000 0.160 X 153743250 missense variant C/T snv 1
rs11146842
ABCD1
1.000 0.160 X 153743056 missense variant G/A snv 1
rs1131691743
ABCD1 ; BCAP31
1.000 0.160 X 153726027 missense variant C/T snv 1
rs1131691916
ABCD1 ; BCAP31
1.000 0.160 X 153725831 missense variant C/T snv 1
rs1131691954
ABCD1 ; BCAP31
1.000 0.160 X 153726146 missense variant G/A snv 1
rs1170974058
ABCD1
1.000 0.160 X 153743495 stop gained C/A;T snv 2.8E-05 1
rs128624213
ABCD1 ; BCAP31
1.000 0.160 X 153726137 missense variant G/A snv 1
rs128624214
ABCD1
1.000 0.160 X 153737214 missense variant C/G snv 1
rs128624215
ABCD1
1.000 0.160 X 153736195 missense variant C/G;T snv 1
rs128624216
ABCD1 ; BCAP31
1.000 0.160 X 153725709 missense variant A/G snv 1
rs128624217
BCAP31 ; ABCD1
1.000 0.160 X 153725786 missense variant T/G snv 1
rs128624218
ABCD1 ; BCAP31
1.000 0.160 X 153726062 missense variant G/A snv 1