Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199516560
ABCB1
0.851 0.200 7 87600772 5 prime UTR variant G/A snv 2.1E-05 5
rs122460151
ARSL
0.851 0.280 X 2958423 missense variant C/G snv 7.1E-05 3.8E-05 5
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 5
rs61748420
MECP2
0.851 0.200 X 154031329 missense variant G/A;T 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
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
rs587776690
ATR
0.882 0.280 3 142556439 synonymous variant T/C snv 4
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 4
rs1301785134
ATR
0.925 0.280 3 142556117 missense variant C/T snv 4.0E-06 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
rs1555050165
GRIA4
0.925 0.200 11 105926814 missense variant A/G 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
rs878853147
NLGN3
0.925 0.200 X 71169399 missense variant C/T snv 3
rs121434614
PAK3
0.925 0.200 X 111196570 missense variant G/C snv 3
rs1278838206
PCDH19
0.925 0.200 X 100296654 missense variant C/T snv 1.1E-05 3
rs121918523
PHF8
0.925 0.200 X 54016662 stop gained T/A snv 3
rs587777696
SLC1A1 ; SPATA6L
0.925 0.280 9 4585316 missense variant C/T snv 4.0E-06 3
rs199469705
TECR
0.925 0.200 19 14564841 missense variant C/T snv 3
rs723744
TTR
0.925 0.200 18 31592513 intron variant G/T snv 0.38 3