Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs672601376
LOC105369668 ; GRIN2B
0.925 0.040 12 13608760 missense variant A/C snv 3
rs723744
TTR
0.925 0.200 18 31592513 intron variant G/T snv 0.38 3
rs735555
CDK5R1
0.925 0.080 17 32490432 3 prime UTR variant C/T snv 0.30 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
rs887386390
L2HGDH
0.925 0.120 14 50283990 missense variant T/C snv 3
rs1047322213
PQBP1
1.000 0.120 X 48902470 missense variant G/A snv 2
rs121434612
PAK3
1.000 0.080 X 111142119 missense variant C/T snv 2
rs121917899
PQBP1
1.000 0.080 X 48901944 missense variant A/G snv 2
rs1294642759
FOXP1
1.000 0.080 3 70959372 missense variant C/T snv 2
rs1372862248
GPT2
1.000 0.120 16 46926991 missense variant G/A snv 2
rs1427146168
NUP214
1.000 0.200 9 131140671 stop gained C/T snv 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
rs225010
DIO2
1.000 0.200 14 80205936 intron variant C/T snv 0.51 2
rs225012
DIO2
1.000 0.200 14 80204392 intron variant A/C;G snv 0.51 2
rs255012 1.000 0.200 7 41189487 regulatory region variant T/A;C snv 2
rs267608402
MECP2
1.000 0.200 X 154030650 missense variant G/A snv 2
rs281860639
MIR6894 ; KDM5C
1.000 0.080 X 53199048 stop gained G/T snv 2
rs3758653
DRD4
1.000 0.200 11 636399 upstream gene variant T/C snv 0.20 2
rs387906728
UBE2A
1.000 X 119574743 missense variant G/A snv 2
rs6511901
CC2D1A
1.000 0.200 19 13916839 intron variant C/T snv 0.39 2
rs6530893
TUSC3
1.000 0.200 8 15671068 intron variant T/C snv 0.14 2
rs6994908
TUSC3
1.000 0.200 8 15674943 intron variant T/C snv 0.32 2
rs747138999
GABRA1
1.000 0.040 5 161895753 missense variant G/T snv 2