Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 5
rs199516560
ABCB1
0.851 0.200 7 87600772 5 prime UTR variant G/A snv 2.1E-05 5
rs397514627
CAMK2G
0.882 0.160 10 73842486 missense variant C/A;G snv 5
rs45517305
TSC2
0.851 0.240 16 2081646 stop gained C/A;T snv 5
rs61748420
MECP2
0.851 0.200 X 154031329 missense variant G/A;T snv 5
rs61751444
MECP2
0.882 0.080 X 154030903 missense variant G/A snv 5
rs864309503
MORC2
0.882 0.200 22 30941503 missense variant G/A snv 5
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 4
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 4
rs587776690
ATR
0.882 0.280 3 142556439 synonymous variant T/C snv 4
rs587777570
KIF5C
1.000 2 148947018 missense variant G/A snv 4
rs672601378
GRIN2B ; LOC105369668
0.882 0.040 12 13615149 missense variant C/T snv 4
rs730882213
ADAT3 ; SCAMP4
0.925 0.080 19 1912477 missense variant G/A snv 7.0E-06 4
rs869320632
LMAN2L
0.925 0.040 2 96739883 missense variant C/T snv 4
rs104886492
HSD17B10
1.000 0.120 X 53432410 missense variant A/G snv 3
rs1131692042
RPL10 ; SNORA70
0.925 0.120 X 154399803 missense variant C/T snv 3
rs121434614
PAK3
0.925 0.200 X 111196570 missense variant G/C snv 3
rs121918523
PHF8
0.925 0.200 X 54016662 stop gained T/A snv 3
rs122468181
UPF3B
0.925 0.200 X 119837771 stop gained G/A;T snv 3
rs1282813621
UPF3B
0.925 0.200 X 119837956 missense variant C/T snv 4.8E-05 3
rs1378981995
ARL13B
0.925 0.200 3 94003751 missense variant G/A snv 7.0E-06 3
rs199469705
TECR
0.925 0.200 19 14564841 missense variant C/T snv 3
rs398122368
SMARCB1
0.925 0.040 22 23791772 missense variant G/A;C snv 3
rs61748392
MECP2
0.925 0.200 X 154031418 missense variant T/C snv 3
rs61751367
MECP2
0.925 0.080 X 154030939 stop gained G/A snv 3