Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13113999 1.000 0.040 4 166265894 intergenic variant T/G snv 0.35 1
rs37792 1.000 0.040 5 53348817 intergenic variant G/A snv 0.67 1
rs57403204 1.000 0.040 X 141990766 intron variant A/G snv 3.7E-02 1
rs9870207 1.000 0.040 3 190807727 intergenic variant A/G snv 0.43 1
rs746442213
ALK
1.000 0.040 2 29232307 missense variant C/A;T snv 4.0E-06; 1.2E-05 1
rs199897804
CDKL5
1.000 0.040 X 18604645 missense variant C/A;T snv 4.9E-05 1
rs1279653488
ERN1
1.000 0.040 17 64047898 missense variant G/A snv 7.0E-06 1
rs116046250
GABRG3
1.000 0.040 15 26986803 intron variant T/G snv 1.5E-02 1
rs150293538
LINC01111
1.000 0.040 8 76408119 intron variant C/T snv 1.4E-02 1
rs79079890
LOC105376360 ; LOC107984193
1.000 0.040 10 3641956 intergenic variant T/G snv 0.10 1
rs1411105125
MAST1
1.000 0.040 19 12873875 missense variant C/T snv 1
rs540521894
NTRK1
1.000 0.040 1 156864760 missense variant C/A;T snv 4.0E-06; 5.6E-05 2.1E-05 1
rs66459581
PRPSAP1
1.000 0.040 17 76359184 intron variant C/- del 0.11 1
rs190220654
SLK
1.000 0.040 10 104002988 missense variant G/C snv 1.2E-04 4.2E-05 1
rs1490428165
TEK
1.000 0.040 9 27209192 missense variant C/G;T snv 4.0E-06 1
rs7902587 0.925 0.080 10 103934543 intergenic variant C/T snv 0.11 2
rs8098244
LAMA3
0.925 0.120 18 23825589 intron variant A/C;G snv 2
rs1400482
LINC00824
0.925 0.120 8 128529685 intron variant G/A snv 0.13 2
rs2165109
MIR4435-2HG ; ACOXL
0.925 0.120 2 111061081 intron variant A/C snv 0.25 2
rs144962376
MLLT10
0.925 0.120 10 21589903 intron variant CCCCTT/-;CCCCTTCCCCTT delins 2
rs1879586
PLEKHM1
0.925 0.120 17 45489971 intron variant C/G snv 0.12 2
rs58722170
RSPO1
0.925 0.120 1 37630749 intron variant G/C snv 0.20 2
rs7207826
SKAP1
0.925 0.120 17 48423311 intron variant T/C snv 0.33 2
rs6005807
TTC28 ; LOC101929594
0.925 0.120 22 28538325 intron variant T/C snv 0.89 2
rs10962692 0.925 0.120 9 16915876 upstream gene variant G/A;C snv 3