Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs1126442
GRIN1 ; LOC105376328
1.000 0.040 9 137156924 missense variant G/A snv 0.26 0.24 2
rs12105421
TMEM182
1.000 0.040 2 102959630 intron variant C/T snv 7.8E-02 2
rs12155594
NRG1
1.000 0.040 8 31749079 intron variant C/T snv 7.8E-02 2
rs12196860
COL21A1
1.000 0.040 6 56085576 intron variant G/A snv 0.15 2
rs1341402
DAOA-AS1
1.000 0.040 13 105463160 intron variant T/C snv 0.16 2
rs1893490
MAPK4
1.000 0.040 18 50669431 non coding transcript exon variant T/C snv 0.48 2
rs1959536
TRIM9
1.000 0.040 14 50980053 intron variant T/G snv 9.7E-02 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs245914
CHN2 ; CPVL
1.000 0.040 7 29178543 intron variant G/A;T snv 2
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs3752088
MAPK4
1.000 0.040 18 50714891 intron variant C/A snv 0.51 2
rs3761554
GRIA3
1.000 0.040 X 123183391 upstream gene variant T/C snv 0.21 2
rs3794899
MAPK4
1.000 0.040 18 50719733 intron variant C/T snv 0.81 2
rs3892158
MAPK4
1.000 0.040 18 50674143 intron variant C/T snv 0.69 2
rs4281084
NRG1
1.000 0.040 8 31637858 upstream gene variant G/A snv 0.22 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
rs6081541
SLC24A3
1.000 0.040 20 19232246 intron variant A/G snv 0.20 2
rs6589386 1.000 0.040 11 113573031 intergenic variant C/T snv 0.36 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2