Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2093816
LINC02341
0.882 13 42471900 intron variant C/T snv 0.47 4
rs2181622
LINC02656 ; LINC02649
0.882 10 6349099 intron variant G/A snv 0.59 4
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs240753
LOC105372548
0.882 20 17881170 intergenic variant T/C snv 0.43 4
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs35776863
NEURL4
0.882 17 7323638 intron variant G/A snv 0.14 0.14 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs4821112
UBE2L3
22 21610472 intron variant G/A snv 0.21 4
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs760361706
PPARA
22 46235326 missense variant G/C snv 4.0E-06 4
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs9356551 0.882 6 166986857 intron variant T/C snv 0.42 4
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 3
rs926657
TAGAP ; LOC105378083
6 159042420 non coding transcript exon variant C/G;T snv 3
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs10460003
LINC01882
18 12747013 intron variant C/T snv 0.15 2
rs10752747
MMEL1
1 2593476 intron variant G/T snv 0.41 2