Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777789
TFG
0.882 0.080 3 100744917 missense variant G/A;T snv 4.0E-06 3
rs207482230
TFG
0.882 0.080 3 100748182 missense variant C/T snv 4.0E-06 5
rs387906738
DYNC1H1
0.882 0.080 14 101980506 missense variant A/G snv 3
rs587781253
DYNC1H1
1.000 0.080 14 101985925 missense variant G/A snv 4.0E-06 1
rs121908160
KIF1B
0.882 0.080 1 10258602 missense variant A/T snv 4
rs267606772
DNM2
0.925 0.080 19 10793799 missense variant G/A snv 3
rs199927590
DNM2
1.000 0.080 19 10797424 missense variant A/G snv 1.1E-04 1.0E-04 1
rs121909088
DNM2
0.925 0.080 19 10819992 missense variant A/G snv 3
rs267607145
TRPV4
0.882 0.080 12 109798820 missense variant G/A;T snv 4
rs267607143
TRPV4
0.851 0.080 12 109798823 missense variant G/A snv 7.0E-06 5
rs267607144
TRPV4
0.716 0.360 12 109800665 missense variant C/T snv 17
rs267607146
TRPV4
0.851 0.080 12 109800666 missense variant G/A;T snv 7.0E-06 5
rs1553192091
ATP1A1 ; ATP1A1-AS1
0.925 0.080 1 116395247 missense variant C/A;G snv 2
rs104894351
HSPB8 ; LOC107984440
0.827 0.080 12 119187078 missense variant A/C;G snv 7
rs104894345
LOC107984440 ; HSPB8
0.827 0.080 12 119187080 missense variant G/C;T snv 6
rs121918312
BAG3
0.776 0.160 10 119672373 missense variant C/A;T snv 11
rs28940291
MFN2
0.776 0.080 1 11992660 missense variant G/A snv 4.0E-06 9
rs119103268
MFN2
0.827 0.080 1 11992689 missense variant C/T snv 6
rs28940294
MFN2
0.882 0.080 1 12001423 missense variant G/A snv 4.0E-06 3
rs2236057
MFN2
0.925 0.120 1 12002148 intron variant A/G snv 0.65 0.65 2
rs119103267
MFN2
0.790 0.160 1 12009641 missense variant C/T snv 2.5E-04 2.8E-04 7
rs776497952
DHTKD1
1.000 0.080 10 12117722 missense variant C/A;T snv 2.4E-05 1
rs756880678
LRSAM1
0.925 0.080 9 127501009 splice acceptor variant G/A snv 2.0E-05 2.8E-05 2
rs786200930
LRSAM1
0.925 0.080 9 127502846 frameshift variant -/GC delins 2
rs119483085
NDRG1
0.851 0.160 8 133258374 stop gained G/A snv 7.0E-06 5