Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1429264
COTL1
1.000 0.040 16 84589878 intron variant T/C snv 0.28 2
rs148173957
LOC105378976
1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 2
rs2071197
HNF4A
0.925 0.120 20 44401795 intron variant G/A snv 0.11 2
rs2304016
SCN2A
0.925 0.040 2 165311993 intron variant A/G snv 1.2E-02 4.8E-03 2
rs2499697
GRM4
0.925 0.040 6 34077141 intron variant A/C;G snv 2
rs3773364
SYN2
0.925 0.040 3 12148468 intron variant A/G snv 0.15 2
rs4817027
MIR155HG
0.925 0.040 21 25566677 intron variant G/A snv 0.59 2
rs55949311
LOC105370210
1.000 0.040 13 53557781 intron variant G/A;T snv 2
rs62270313
EPHB1
1.000 0.040 3 134930924 intron variant T/C snv 0.16 2
rs631844
LINC02109 ; LOC107986410
1.000 0.040 5 29054513 intron variant C/T snv 0.48 2
rs7171755
REC114
0.925 0.120 15 73558239 intron variant G/A snv 0.45 2
rs7328626 1.000 0.040 13 53576772 intron variant G/A;T snv 2
rs79007183
CRAMP1
1.000 0.040 16 1655793 intron variant G/A snv 2.8E-05 2
rs9596837 1.000 0.040 13 53683928 intron variant T/C snv 0.11 2
rs9596863
LINC00558
1.000 0.040 13 53860512 intron variant T/G snv 0.11 2
rs987195
MIR155HG
0.925 0.040 21 25565010 intron variant C/G;T snv 2
rs10030601
IQCM
1.000 0.040 4 149804060 intron variant T/C snv 0.22 1
rs10234411
ABCB1
1.000 0.040 7 87535576 intron variant T/A;C;G snv 1
rs1109771
NOTCH4
1.000 0.040 6 32219828 intron variant A/G snv 0.57 0.54 1
rs11214136
BCO2
1.000 0.040 11 112211286 intron variant T/C snv 0.12 1
rs1394074
OLFML3
1.000 0.040 1 114005041 intron variant C/G snv 2.9E-02 1
rs2278637
VAMP2
1.000 0.040 17 8158784 intron variant G/T snv 0.67 1
rs3815824
MVP
1.000 0.040 16 29841539 intron variant C/T snv 0.16 1
rs39861
MAST4
1.000 0.040 5 66856430 intron variant A/G snv 0.25 1
rs42938
GAL3ST1
1.000 0.040 22 30569770 intron variant T/C snv 0.41 1