Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1245554802
CAMK1 ; OGG1
0.851 0.120 3 9765892 splice acceptor variant T/C snv 4.0E-06 5
rs771306418
CAMK1 ; OGG1
0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs9302001
LOC101927284
1.000 0.040 13 94811138 intergenic variant C/A;T snv 1
rs324891
LINC00461
1.000 0.040 5 88616114 intron variant C/T snv 4.2E-04 1
rs7788
SNAPC2
1.000 0.040 19 7923232 3 prime UTR variant T/C snv 0.28 1
rs4804833
MAP2K7
1.000 0.040 19 7905750 intron variant A/G;T snv 1
rs3816995
SDK2
1.000 0.040 17 73339121 intron variant G/A snv 0.40 1
rs10879357
TPH2
1.000 0.040 12 72020783 intron variant A/G snv 0.59 1
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs1487275
TPH2
1.000 0.040 12 72016512 intron variant C/A snv 0.71 1
rs4760820
TPH2
0.925 0.040 12 72003216 intron variant C/G snv 0.29 2
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs11179000
TPH2
0.925 0.040 12 71944848 intron variant A/T snv 0.31 2
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4448731 1.000 0.040 12 71935326 upstream gene variant T/C snv 0.40 1
rs1418688 1.000 0.040 6 71169166 downstream gene variant A/G;T snv 1
rs10454453
PDE4B
1.000 0.040 1 66206849 intron variant C/A snv 0.48 1
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs7301616 1.000 0.040 12 60214608 intron variant C/T snv 0.96 1
rs12579350
ANO2
0.882 0.080 12 5687935 intron variant G/A snv 0.12 3
rs1805067
SLC6A2
0.925 0.080 16 55698511 missense variant G/A snv 2.8E-05 2.1E-05 2