Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1341402
DAOA-AS1
1.000 0.040 13 105463160 intron variant T/C snv 0.16 2
rs701492
GAD1
1.000 0.040 2 170845970 intron variant C/T snv 0.30 0.28 2
rs769404
GAD1
1.000 0.040 2 170822115 synonymous variant T/C snv 0.39 0.35 2
rs3761554
GRIA3
1.000 0.040 X 123183391 upstream gene variant T/C snv 0.21 2
rs502434
GRIA3
1.000 0.040 X 123403426 synonymous variant T/C snv 0.59 2
rs1126442
GRIN1 ; LOC105376328
1.000 0.040 9 137156924 missense variant G/A snv 0.26 0.24 2
rs1893490
MAPK4
1.000 0.040 18 50669431 non coding transcript exon variant T/C snv 0.48 2
rs3752088
MAPK4
1.000 0.040 18 50714891 intron variant C/A snv 0.51 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
rs12155594
NRG1
1.000 0.040 8 31749079 intron variant C/T snv 7.8E-02 2
rs4281084
NRG1
1.000 0.040 8 31637858 upstream gene variant G/A snv 0.22 2
rs713729
PICK1
1.000 0.040 22 38059462 intron variant T/A snv 0.20 2
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs737864
TXNRD2 ; COMT
1.000 0.040 22 19942636 intron variant C/T snv 0.23 2
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 3
rs2619539
DTNBP1
0.925 0.040 6 15620624 intron variant C/A;G snv 3
rs989638
GRIA3
0.925 0.040 X 123239256 intron variant C/G;T snv 3
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 3
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs7687423
NPY1R
0.925 0.080 4 163329645 intron variant A/G snv 0.53 3
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
rs2076369
PICK1
0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 3