Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs374073809
VASH2
1 212961166 missense variant C/A;G;T snv 4.0E-06; 1.6E-05; 3.2E-05 1
rs374854258
DGCR2
22 19065049 missense variant G/A snv 2.0E-05 3.5E-05 1
rs551253128
MID2 ; LOC101928335
X 107905581 missense variant A/G snv 1.3E-03 1.6E-04 1
rs749451963
DGCR2
22 19064948 missense variant C/T snv 4.0E-06 1
rs753303079
CD55
1 207325673 missense variant C/G;T snv 8.0E-06 1
rs761249181
COL9A1
6 70252139 missense variant C/T snv 1.6E-05 1
rs879255635
ZBTB20
3 114339384 missense variant G/A snv 1
rs930549037
COL9A2
1 40301333 missense variant C/T snv 4.4E-05 2.8E-05 1
rs968910165
NCAM2
21 21286370 missense variant A/G;T snv 4.0E-06 1.4E-05 1
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs672601378
GRIN2B ; LOC105369668
0.882 0.040 12 13615149 missense variant C/T snv 4
rs869320632
LMAN2L
0.925 0.040 2 96739883 missense variant C/T snv 4
rs398122368
SMARCB1
0.925 0.040 22 23791772 missense variant G/A;C snv 3
rs672601376
LOC105369668 ; GRIN2B
0.925 0.040 12 13608760 missense variant A/C snv 3
rs781442277
PTRHD1 ; CENPO ; LOC105369164
1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs1445362103
ARHGEF7
1.000 0.040 13 111244248 missense variant T/C snv 1.2E-05 7.0E-06 2
rs145390085
L2HGDH
1.000 0.040 14 50269297 missense variant A/G snv 2
rs1882260
NLGN4X
1.000 0.040 X 5890820 3 prime UTR variant G/A snv 2
rs747138999
GABRA1
1.000 0.040 5 161895753 missense variant G/T snv 2
rs774843232
PGAP2
0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 9
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs1162306056
KCNQ3
0.882 0.080 8 132174294 missense variant C/T snv 5
rs142698837
TG
0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 5
rs398122917
CLIC2
0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 5
rs61751444
MECP2
0.882 0.080 X 154030903 missense variant G/A snv 5