Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518848
TCF4
0.827 0.240 18 55229003 frameshift variant -/ATTG delins 15
rs1057519429
CACNA1A
0.807 0.240 19 13235666 missense variant C/G;T snv 15
rs864309488
GMNN
0.776 0.440 6 24777296 missense variant A/G snv 14
rs869312824
GNB1
0.827 0.200 1 1804565 missense variant A/G snv 14
rs913477149
RFT1
0.851 0.160 3 53105728 missense variant T/A;C snv 13
rs1555570093
MPDU1
0.807 0.280 17 7586699 missense variant G/A snv 12
rs758946412
PCDH19
0.790 0.240 X 100407507 frameshift variant G/-;GG delins 12
rs1060499733
DHX30
0.851 0.120 3 47846757 missense variant A/G snv 11
rs869025195
RIT1
0.790 0.280 1 155904493 missense variant T/G snv 11
rs1555483699
GRIN2A
0.851 0.120 16 9768994 missense variant C/T snv 10
rs755604487
PHIP
0.790 0.200 6 79026079 stop gained G/A;C snv 10
rs1325394060
HUWE1
0.851 0.320 X 53534144 missense variant C/G;T snv 9.5E-06 9
rs1555570110
MPDU1
0.827 0.240 17 7586766 missense variant A/C snv 9
rs869312823
GNB1
0.882 0.080 1 1806509 missense variant T/C snv 9
rs1553196101
CDC42
0.925 0.080 1 22086507 missense variant T/C snv 8
rs1564341846
POMT1
0.790 0.280 9 131508926 missense variant C/A snv 8
rs869312822
GNB1
0.827 0.200 1 1806514 missense variant A/C snv 8
rs1057518681
PUF60 ; SCRIB
0.827 0.200 8 143816821 splice acceptor variant T/C snv 7
rs1057519436
DHX30
0.882 0.200 3 47846550 missense variant G/A snv 7
rs1057519443
MPP4
0.882 0.200 2 201675255 missense variant A/G snv 7
rs1556913258
HUWE1
0.851 0.280 X 53536580 missense variant G/C snv 7
rs1556978515
HUWE1
0.851 0.280 X 53591113 missense variant T/C snv 7
rs1567815105
ADGRG1
0.807 0.240 16 57660794 frameshift variant -/T delins 7
rs886041876
HUWE1
0.851 0.280 X 53551078 missense variant G/A snv 7
rs1553196134
CDC42
0.925 0.080 1 22086856 missense variant C/T snv 6