Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13333659
CBFA2T3
1.000 0.040 16 88972472 intron variant G/T snv 0.13 2
rs17601241
MIR4713HG ; CYP19A1
1.000 0.040 15 51215677 intron variant G/A snv 0.11 8.6E-02 2
rs2162560
DNMT1
1.000 0.040 19 10168778 intron variant G/A snv 0.35 2
rs2283368
KL
1.000 0.040 13 33019132 intron variant T/C snv 0.15 2
rs469083
MX1
1.000 0.040 21 41436789 intron variant C/T snv 0.61 2
rs9526984
KL
1.000 0.040 13 33035800 intron variant A/G snv 5.5E-02 2
rs10512015
ANXA1
9 73166330 intron variant T/C snv 9.9E-02 1
rs17641411
GABRA4
4 46941670 intron variant C/T snv 2.8E-02 1
rs2973488
CTNND2
5 11043805 intron variant A/T snv 0.19 1
rs73643144
TEK
9 27126454 intron variant T/C snv 3.5E-02 1
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs16885997 8 114496877 intergenic variant G/T snv 3.5E-02 1
rs7700443 5 85876294 intergenic variant T/G snv 0.57 1
rs555145190
NAGLU
0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs1555377415
IRF2BPL ; LOC107984638
0.827 0.200 14 77027274 stop gained G/C snv 18
rs1555454508
SPG11
0.790 0.240 15 44615487 stop gained GTA/ATC mnv 18
rs765061840
SPG11
0.882 0.120 15 44633619 stop gained G/A snv 1.2E-05 7.0E-06 6
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135