Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1249144069
PITRM1-AS1 ; PITRM1
0.925 0.200 10 3165320 missense variant C/T snv 1.4E-05 5
rs121918364
SRPX2
0.851 0.200 X 100662227 missense variant A/C snv 3.3E-05 2.9E-05 5
rs142698837
TG
0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 5
rs45517305
TSC2
0.851 0.240 16 2081646 stop gained C/A;T snv 5
rs1404008939
ABCB1
0.925 0.200 7 87504324 missense variant A/C;G snv 4.0E-06 4
rs730882213
ADAT3 ; SCAMP4
0.925 0.080 19 1912477 missense variant G/A snv 7.0E-06 4
rs587776690
ATR
0.882 0.280 3 142556439 synonymous variant T/C snv 4
rs672601378
GRIN2B ; LOC105369668
0.882 0.040 12 13615149 missense variant C/T snv 4
rs587777570
KIF5C
1.000 2 148947018 missense variant G/A snv 4
rs869320632
LMAN2L
0.925 0.040 2 96739883 missense variant C/T snv 4
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
rs1378981995
ARL13B
0.925 0.200 3 94003751 missense variant G/A snv 7.0E-06 3
rs1301785134
ATR
0.925 0.280 3 142556117 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
rs121918368
CRBN ; TRNT1
0.925 0.200 3 3150939 stop gained G/A snv 8.0E-06 7.0E-06 3
rs752306
DRD4
0.925 0.200 11 637622 intron variant C/T snv 6.4E-02 4.8E-02 3
rs132630328
GK
0.925 0.200 X 30720721 missense variant A/G;T snv 5.4E-06 3
rs104886492
HSD17B10
1.000 0.120 X 53432410 missense variant A/G snv 3
rs887386390
L2HGDH
0.925 0.120 14 50283990 missense variant T/C snv 3
rs672601376
LOC105369668 ; GRIN2B
0.925 0.040 12 13608760 missense variant A/C snv 3
rs61748392
MECP2
0.925 0.200 X 154031418 missense variant T/C snv 3
rs61749735
MECP2
0.925 0.200 X 154031162 synonymous variant G/A;C snv 5.4E-06; 3.8E-05 3