Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs185645212
POLG
0.851 0.240 15 89323504 missense variant C/A;T snv 8.0E-06; 9.7E-04 6
rs5030849
PAH
0.851 0.280 12 102852875 missense variant C/A;G;T snv 2.2E-04 6
rs863225264
MTOR
0.827 0.240 1 11130747 missense variant C/T snv 6
rs878854402
TBL1XR1
0.851 0.280 3 177033050 missense variant T/C snv 6
rs886041761
KCNA2
0.925 0.200 1 110603902 missense variant C/T snv 6
rs1162306056
KCNQ3
0.882 0.080 8 132174294 missense variant C/T snv 5
rs1364926780
ABCB1
0.882 0.200 7 87550272 missense variant C/T snv 5
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 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
rs121434613
PAK3
0.882 0.240 X 111194402 missense variant C/A snv 4
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
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
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
rs1278838206
PCDH19
0.925 0.200 X 100296654 missense variant C/T snv 1.1E-05 3