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
rs28928910
NEFL
0.827 0.200 8 24956452 missense variant G/A;T snv 11
rs121913586
MPZ
0.752 0.200 1 161306414 missense variant C/G;T snv 10
rs58982919
NEFL
0.790 0.080 8 24956223 missense variant T/C snv 10
rs104894619
PMP22
0.827 0.120 17 15231047 missense variant G/A snv 4.0E-03 3.7E-03 9
rs104894621
PMP22
0.790 0.080 17 15239575 missense variant G/A snv 9
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
rs104894161
EGR2
0.807 0.080 10 62813563 missense variant G/A snv 6
rs104894159
EGR2
0.827 0.080 10 62813413 missense variant G/A snv 5
rs121913590
MPZ
0.851 0.080 1 161306864 missense variant G/A snv 7.0E-06 5
rs121913598
MPZ
0.851 0.080 1 161307361 missense variant G/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
rs281865137
EGR2
0.851 0.080 10 62813496 missense variant C/T snv 4
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
rs104894617
PMP22
0.851 0.080 17 15260681 missense variant A/G snv 4
rs104894623
PMP22
0.851 0.200 17 15239591 missense variant C/G;T snv 4