Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607144
TRPV4
0.716 0.360 12 109800665 missense variant C/T snv 17
rs137852973
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.200 11 62702493 missense variant G/A;C snv 7.0E-06 13
rs121913595
MPZ
0.742 0.160 1 161306785 missense variant G/A;T snv 11
rs121918312
BAG3
0.776 0.160 10 119672373 missense variant C/A;T snv 11
rs58982919
NEFL
0.790 0.080 8 24956223 missense variant T/C snv 10
rs104894621
PMP22
0.790 0.080 17 15239575 missense variant G/A snv 9
rs104894351
HSPB8 ; LOC107984440
0.827 0.080 12 119187078 missense variant A/C;G snv 7
rs1553259662
MPZ
0.827 0.200 1 161306821 missense variant A/G snv 7
rs397515323
PDK3
0.851 0.080 X 24503479 missense variant G/A snv 7
rs104894161
EGR2
0.807 0.080 10 62813563 missense variant G/A snv 6
rs104894345
LOC107984440 ; HSPB8
0.827 0.080 12 119187080 missense variant G/C;T snv 6
rs119103268
MFN2
0.827 0.080 1 11992689 missense variant C/T snv 6
rs104894078
GDAP1
0.851 0.080 8 74360184 missense variant C/T snv 7.0E-06 5
rs104894158
EGR2
0.851 0.080 10 62813835 missense variant A/T snv 5
rs104894159
EGR2
0.827 0.080 10 62813413 missense variant G/A snv 5
rs119483085
NDRG1
0.851 0.160 8 133258374 stop gained G/A snv 7.0E-06 5
rs121913597
MPZ
0.827 0.160 1 161307268 missense variant T/A snv 5
rs121913602
MPZ
0.851 0.120 1 161307308 missense variant T/A snv 5
rs267607143
TRPV4
0.851 0.080 12 109798823 missense variant G/A snv 7.0E-06 5
rs267607146
TRPV4
0.851 0.080 12 109800666 missense variant G/A;T snv 7.0E-06 5
rs281865128
MPZ
0.882 0.080 1 161306426 missense variant C/G;T snv 5
rs58332872
NEFL
0.882 0.080 8 24956248 missense variant C/T snv 5
rs864309503
MORC2
0.882 0.200 22 30941503 missense variant G/A snv 5
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