Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913603
MPZ
0.732 0.160 1 161306722 missense variant T/C;G snv 2.0E-05 12
rs121913595
MPZ
0.742 0.160 1 161306785 missense variant G/A;T snv 11
rs121913586
MPZ
0.752 0.200 1 161306414 missense variant C/G;T snv 10
rs1553259648
MPZ
0.776 0.160 1 161306759 missense variant G/C;T snv 8
rs121913589
MPZ
0.827 0.200 1 161306863 missense variant C/A;G;T snv 7
rs1553259662
MPZ
0.827 0.200 1 161306821 missense variant A/G snv 7
rs121913590
MPZ
0.851 0.080 1 161306864 missense variant G/A snv 7.0E-06 5
rs121913597
MPZ
0.827 0.160 1 161307268 missense variant T/A snv 5
rs121913598
MPZ
0.851 0.080 1 161307361 missense variant G/A snv 5
rs121913602
MPZ
0.851 0.120 1 161307308 missense variant T/A snv 5
rs281865127
MPZ
0.827 0.120 1 161306767 missense variant T/C snv 5
rs281865128
MPZ
0.882 0.080 1 161306426 missense variant C/G;T snv 5
rs371856018
MPZ
0.882 0.120 1 161307376 missense variant T/C;G snv 8.0E-06 5
rs121913585
MPZ
0.851 0.080 1 161307304 missense variant G/A;C snv 4
rs121913596
MPZ
0.851 0.080 1 161307389 missense variant C/A;T snv 4.0E-06 4
rs121913601
MPZ
0.851 0.080 1 161307259 missense variant G/A;C snv 4
rs1553259707
MPZ
0.851 0.080 1 161306911 missense variant T/C snv 4
rs572010627
MPZ
0.851 0.160 1 161306738 missense variant A/C;T snv 8.0E-06 4
rs121913584
MPZ
0.925 0.080 1 161306886 missense variant G/A;C;T snv 3.2E-05 3
rs121913594
MPZ
0.882 0.080 1 161306914 missense variant T/C snv 3
rs121913599
MPZ
0.882 0.080 1 161306763 missense variant G/T snv 3
rs267607247
MPZ
0.882 0.120 1 161305953 missense variant C/A snv 3
rs770546306
MPZ
0.882 0.080 1 161307402 missense variant G/A;C;T snv 3.2E-05; 5.2E-05 3
rs797044845
MPZ
0.882 0.080 1 161307311 missense variant C/T snv 3
rs879253858
MPZ
0.882 0.120 1 161306753 missense variant T/G snv 3