Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557935477
POGZ
1.000 0.040 1 151440939 missense variant G/T snv 1
rs587777457
MAOA
0.925 0.200 X 43731695 missense variant G/T snv 1
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 2
rs121918799
SCN1A-AS1 ; SCN1A ; LOC102724058
0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 2
rs1557901347
POGZ
1.000 0.040 1 151424027 missense variant G/C snv 1
rs1557902023
POGZ
1.000 0.040 1 151424154 missense variant G/C snv 1
rs1557909572
POGZ
1.000 0.040 1 151427931 missense variant G/C snv 1
rs574335012
POGZ
1.000 0.040 1 151427959 missense variant G/C snv 1.2E-05 1
rs778792467
POGZ
1.000 0.040 1 151405692 missense variant G/C snv 4.4E-05 7.0E-06 1
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 12
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 2
rs121912562
NR3C2
0.925 0.160 4 148435252 stop gained G/A;C snv 4.0E-06 2
rs1396313317
CNTNAP2 ; LOC107986721
1.000 0.040 7 147562137 splice acceptor variant G/A;C snv 4.0E-06 1
rs1476293577
POGZ
1.000 0.040 1 151428188 missense variant G/A;C snv 1
rs998675361
POGZ
1.000 0.040 1 151430806 missense variant G/A;C snv 9.0E-06 1
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 11
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23 2
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 2
rs886037776
EHMT1
0.925 0.280 9 137817477 stop gained G/A snv 2
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs1372713010
POGZ
1.000 0.040 1 151428041 missense variant G/A snv 1
rs1557867853
POGZ
1.000 0.040 1 151406330 missense variant G/A snv 1