Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 4
rs121913595
MPZ
0.742 0.160 1 161306785 missense variant G/A;T snv 4
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs281865127
MPZ
0.827 0.120 1 161306767 missense variant T/C snv 3
rs28940291 0.776 0.080 1 11992660 missense variant G/A snv 4.0E-06 3
rs57520892 0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 3
rs60890628 0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 3
rs80359818 0.776 0.360 1 42930766 missense variant G/A snv 3
rs1762111 0.851 0.080 1 94021934 missense variant A/G snv 1.2E-03 1.3E-03 3
rs121434595 0.708 0.320 1 114716124 missense variant C/A;G;T snv 2
rs121913586
MPZ
0.752 0.200 1 161306414 missense variant C/G;T snv 2
rs879253858
MPZ
0.882 0.120 1 161306753 missense variant T/G snv 2
rs121913585
MPZ
0.851 0.080 1 161307304 missense variant G/A;C snv 2
rs121913590
MPZ
0.851 0.080 1 161306864 missense variant G/A snv 7.0E-06 2
rs1553259707
MPZ
0.851 0.080 1 161306911 missense variant T/C snv 2
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 2
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 2
rs74315368 0.882 0.080 1 17022648 missense variant C/T snv 1.2E-05 1.4E-05 2
rs772551056 0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 2
rs60652225 0.851 0.200 1 156130679 missense variant T/C;G snv 2
rs142000963 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 2
rs1442918125 0.925 0.080 1 21575907 missense variant G/A snv 8.0E-06 7.0E-06 2
rs199669988 0.882 0.080 1 21564097 missense variant G/A snv 1.3E-04 3.5E-05 2
rs766076920 0.882 0.080 1 21568122 missense variant C/T snv 8.0E-06 2.1E-05 2
rs121918001 0.882 0.080 1 21561126 missense variant C/A;T snv 2