Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs796052571
GRIN2B ; LOC105369668
0.851 0.040 12 13608755 missense variant C/T snv 6
rs1057521223
SCN2A
1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs587777162
EEF1A2
0.925 0.040 20 63495972 missense variant C/T snv 5
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1568070621
BPTF
1.000 0.040 17 67918746 frameshift variant AG/- delins 4
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 3
rs1057519440
GSPT2
1.000 0.040 X 51744647 missense variant G/A snv 3
rs11585926
TRIM33
1.000 0.040 1 114431068 intron variant T/C snv 0.22 3
rs201551401
GPR37
0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs3747333
NLGN4X
0.925 0.040 X 5893491 missense variant G/A;C;T snv 7.6E-03 3
rs3747334
NLGN4X
0.925 0.040 X 5893489 synonymous variant G/A;C;T snv 1.2E-05; 6.7E-03 3
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs850807 0.882 0.040 15 23652982 intergenic variant T/A;C snv 3
rs10951154
HOTAIRM1 ; HOXA1
0.925 0.040 7 27095695 missense variant C/A;G;T snv 0.76 2
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs11179000
TPH2
0.925 0.040 12 71944848 intron variant A/T snv 0.31 2