Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
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
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
rs3740360
PLCE1
0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 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
rs3132468
MICB
0.827 0.240 6 31507709 intron variant C/T snv 0.77 5
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
rs281865127
MPZ
0.827 0.120 1 161306767 missense variant T/C snv 5
rs104894708
PRX
0.851 0.120 19 40395144 stop gained G/A snv 8.0E-06 5
rs121913585
MPZ
0.851 0.080 1 161307304 missense variant G/A;C snv 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
rs104894617
PMP22
0.851 0.080 17 15260681 missense variant A/G snv 4
rs879253954
PMP22
0.882 0.160 17 15230951 missense variant C/A;T snv 4
rs104894707
PRX
0.882 0.080 19 40396207 stop gained A/T snv 8.0E-06 5.6E-05 4
rs104894826
GJB1
0.882 0.080 X 71224114 missense variant T/C snv 3
rs770546306
MPZ
0.882 0.080 1 161307402 missense variant G/A;C;T snv 3.2E-05; 5.2E-05 3