Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1466835565
HK1
10 69368539 missense variant A/G snv 1
rs1553510492
TBR1
2 161419040 missense variant A/G snv 4
rs1554121671
SYNGAP1
1.000 6 33440746 frameshift variant -/AGGA delins 4
rs1554776954
STXBP1
1.000 9 127661133 frameshift variant A/- delins 5
rs1555103646
GRIN2B
1.000 0.040 12 13569964 missense variant C/A snv 4
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs1555462347
USP7
0.716 0.520 16 8901028 frameshift variant CT/- delins 34
rs1561515242
CAMK4
1.000 0.080 5 111482938 splice donor variant G/A snv 6
rs1569355102
DYRK1A
0.695 0.360 21 37472869 frameshift variant TAAC/- delins 51
rs1799920
HTR1A
5 63961656 missense variant C/G;T snv 3.2E-04 2
rs1799921
HTR1A
5 63961638 missense variant T/C snv 9.4E-03 9.3E-03 2
rs1800014
PRNP
0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs1800044
HTR1A
0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs200754713
PSEN2
1 226888954 missense variant A/G snv 4.0E-06; 4.0E-06 2
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2049161
DLGAP1
18 4127583 intron variant A/C;T snv 0.22 2
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs2144025
ESR1
0.925 0.080 6 151986571 intron variant T/A;C snv 4