Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052108705
TCF19 ; POU5F1
6 31165217 missense variant C/T snv 4.1E-06 2.1E-05 3
rs1131692042
RPL10 ; SNORA70
0.925 0.120 X 154399803 missense variant C/T snv 3
rs1278838206
PCDH19
0.925 0.200 X 100296654 missense variant C/T snv 1.1E-05 3
rs1282813621
UPF3B
0.925 0.200 X 119837956 missense variant C/T snv 4.8E-05 3
rs1301785134
ATR
0.925 0.280 3 142556117 missense variant C/T snv 4.0E-06 3
rs140032597
UPF3B
0.925 0.200 X 119837923 missense variant C/T snv 6.6E-05 1.1E-04 3
rs199469705
TECR
0.925 0.200 19 14564841 missense variant C/T snv 3
rs587777696
SLC1A1 ; SPATA6L
0.925 0.280 9 4585316 missense variant C/T snv 4.0E-06 3
rs735555
CDK5R1
0.925 0.080 17 32490432 3 prime UTR variant C/T snv 0.30 3
rs752306
DRD4
0.925 0.200 11 637622 intron variant C/T snv 6.4E-02 4.8E-02 3
rs768746587
TCF19 ; POU5F1
6 31165136 missense variant C/T snv 8.4E-06 3
rs781442277
PTRHD1 ; CENPO ; LOC105369164
1.000 0.040 2 24793223 missense variant C/T snv 4.0E-06; 1.2E-05 3
rs786201003
NALCN
0.925 0.080 13 101083752 missense variant C/T snv 3
rs878853147
NLGN3
0.925 0.200 X 71169399 missense variant C/T snv 3
rs115466046
KCNJ10
1 160042480 missense variant C/T snv 1.2E-02 1.1E-02 2
rs121434612
PAK3
1.000 0.080 X 111142119 missense variant C/T snv 2
rs1294642759
FOXP1
1.000 0.080 3 70959372 missense variant C/T snv 2
rs1335072648
RAD21
1.000 0.200 8 116854423 missense variant C/T snv 4.0E-06 2
rs140646329
KCNJ10
1 160042283 missense variant C/T snv 2.0E-05 1.4E-05 2
rs1427146168
NUP214
1.000 0.200 9 131140671 stop gained C/T snv 2
rs1438466809
KCNJ1
11 128840191 missense variant C/T snv 4.0E-06 2
rs202198533
MYH2 ; MYHAS
17 10533547 missense variant C/T snv 1.6E-04 1.0E-04 2
rs225010
DIO2
1.000 0.200 14 80205936 intron variant C/T snv 0.51 2
rs370667926
MED23
1.000 6 131603129 missense variant C/T snv 1.6E-05 1.4E-05 2
rs6511901
CC2D1A
1.000 0.200 19 13916839 intron variant C/T snv 0.39 2