Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 3
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs1992044
LOC105375856 ; LINC01602
8 57928349 intron variant G/A;T snv 2
rs245914
CHN2 ; CPVL
1.000 0.040 7 29178543 intron variant G/A;T snv 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs502434
GRIA3
1.000 0.040 X 123403426 synonymous variant T/C snv 0.59 2
rs5905512
MAOB
1.000 0.040 X 43867148 intron variant A/G snv 2
rs7065696
PHF8
X 53947621 intron variant C/G;T snv 2
rs751229
DISC1 ; TSNAX-DISC1
1.000 0.040 1 231632793 intron variant A/G;T snv 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs1249144069
PITRM1-AS1 ; PITRM1
0.925 0.200 10 3165320 missense variant C/T snv 1.4E-05 5
rs61749465
MCPH1
0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 3
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4