Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs737864
TXNRD2 ; COMT
1.000 0.040 22 19942636 intron variant C/T snv 0.23 2
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 3
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 3
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs3788533
PLA2G6
0.925 0.040 22 38127239 non coding transcript exon variant C/G snv 0.47 3
rs1249144069
PITRM1-AS1 ; PITRM1
0.925 0.200 10 3165320 missense variant C/T snv 1.4E-05 5
rs2076369
PICK1
0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 3
rs713729
PICK1
1.000 0.040 22 38059462 intron variant T/A snv 0.20 2
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs3924999
NRG1
0.851 0.040 8 32595840 missense variant G/A snv 0.40 0.31 5
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
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
rs7687423
NPY1R
0.925 0.080 4 163329645 intron variant A/G snv 0.53 3
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174