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
rs121913603
MPZ
0.732 0.160 1 161306722 missense variant T/C;G snv 2.0E-05 8
rs121913597
MPZ
0.827 0.160 1 161307268 missense variant T/A snv 4
rs121913599
MPZ
0.882 0.080 1 161306763 missense variant G/T snv 2
rs121913602
MPZ
0.851 0.120 1 161307308 missense variant T/A snv 2
rs1553259643
MPZ
0.925 0.080 1 161306719 frameshift variant TACA/- delins 2
rs1553259662
MPZ
0.827 0.200 1 161306821 missense variant A/G snv 2
rs1553259703
MPZ
0.925 0.080 1 161306900 stop gained G/A snv 2
rs281865128
MPZ
0.882 0.080 1 161306426 missense variant C/G;T snv 2
rs572010627
MPZ
0.851 0.160 1 161306738 missense variant A/C;T snv 8.0E-06 2
rs863225026
MPZ
0.925 0.080 1 161305973 splice acceptor variant TCTGGGGGAGGGGCG/- delins 2
rs121913608
MPZ
0.925 0.080 1 161306789 missense variant C/T snv 1
rs1553259760
MPZ
0.925 0.080 1 161307299 missense variant T/C snv 1
rs760730366
MPZ
1.000 0.080 1 161307356 frameshift variant GGGAGCCC/- delins 1.2E-05 1
rs879254038
MPZ
0.925 0.080 1 161306800 missense variant T/C snv 1