Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913595
MPZ
0.742 0.160 1 161306785 missense variant G/A;T snv 10
rs121913586
MPZ
0.752 0.200 1 161306414 missense variant C/G;T snv 9
rs121913603
MPZ
0.732 0.160 1 161306722 missense variant T/C;G snv 2.0E-05 8
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
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
rs121913597
MPZ
0.827 0.160 1 161307268 missense variant T/A snv 4
rs1553259707
MPZ
0.851 0.080 1 161306911 missense variant T/C snv 4
rs281865127
MPZ
0.827 0.120 1 161306767 missense variant T/C snv 4
rs121913590
MPZ
0.851 0.080 1 161306864 missense variant G/A snv 7.0E-06 3
rs121913594
MPZ
0.882 0.080 1 161306914 missense variant T/C snv 3
rs121913598
MPZ
0.851 0.080 1 161307361 missense variant G/A snv 3
rs121913601
MPZ
0.851 0.080 1 161307259 missense variant G/A;C snv 3
rs121913583
MPZ
0.925 0.080 1 161306870 missense variant T/C snv 2
rs121913584
MPZ
0.925 0.080 1 161306886 missense variant G/A;C;T snv 3.2E-05 2
rs121913588
MPZ
0.925 0.080 1 161306747 missense variant C/T snv 2
rs121913599
MPZ
0.882 0.080 1 161306763 missense variant G/T snv 2
rs121913600
MPZ
0.925 0.080 1 161306848 missense variant C/T snv 2
rs121913602
MPZ
0.851 0.120 1 161307308 missense variant T/A snv 2
rs1553259662
MPZ
0.827 0.200 1 161306821 missense variant A/G snv 2
rs1553259790
MPZ
0.925 0.080 1 161307340 missense variant G/A snv 2
rs1558154193
MPZ
0.925 0.080 1 161306880 synonymous variant C/T snv 2
rs267607247
MPZ
0.882 0.120 1 161305953 missense variant C/A snv 2
rs281865124
MPZ
0.925 0.080 1 161306912 missense variant A/G snv 2