Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141441277
SYTL4
0.882 0.120 X 100689933 missense variant G/A snv 5.6E-04 3.8E-04 5
rs2078178
CLEC7A ; LOC105369655
1.000 0.040 12 10123963 intron variant A/G snv 0.55 1
rs10418707
DNMT1
1.000 0.040 19 10145541 intron variant G/A;T snv 0.11 1
rs10423341
DNMT1
1.000 0.040 19 10156590 intron variant C/A snv 0.13 1
rs3213607
GRIK2
0.925 0.080 6 102035481 synonymous variant C/A;T snv 6.5E-02; 2.0E-05 2
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs35678
ATP2B2
0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47 2
rs241509
ATP2B2
1.000 0.040 3 10345375 intron variant C/A;T snv 0.45 1
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs1275980031
RELN
1.000 0.040 7 103540259 missense variant G/A snv 4.0E-06 2
rs3774180
ATP2B2
1.000 0.040 3 10355304 intron variant T/C snv 0.37 1
rs2278556
ATP2B2
0.925 0.040 3 10360419 intron variant G/A snv 0.34 2
rs362691
RELN
0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12 3
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs2237659
COG5
1.000 0.040 7 107207047 intron variant T/G snv 0.19 1
rs2158836
LAMB1
1.000 0.040 7 107940394 non coding transcript exon variant A/G snv 0.63 0.64 1
rs20556
LAMB1
1.000 0.040 7 107953544 missense variant T/C snv 0.65 0.66 1
rs25659
LAMB1
1.000 0.040 7 107986325 synonymous variant G/A snv 0.12 0.11 1
rs3918346
DAO
0.925 0.040 12 108888108 intron variant G/A snv 0.34 2
rs3825251
DAO
0.925 0.040 12 108894208 intron variant A/G snv 0.18 2
rs17606561
ELOVL2
1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 2
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 4
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs9468304
ELOVL2-AS1 ; ELOVL2
1.000 0.040 6 11041932 intron variant G/A snv 0.19 2