Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10042486 0.882 0.040 5 63965502 intron variant C/T snv 0.58 4
rs10070190 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 2
rs11783752 0.925 0.040 8 20192013 intergenic variant G/A;C snv 2
rs12504244 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 2
rs2834070 0.925 0.040 21 33015144 intron variant G/T snv 0.24 2
rs4785741 1.000 0.040 16 89939045 downstream gene variant T/C snv 0.47 2
rs1000592 1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03 1
rs10491734 1.000 0.040 9 4482706 intergenic variant T/A;C snv 1
rs12536521 1.000 0.040 7 89349373 intergenic variant T/A snv 4.8E-02 1
rs12635725 1.000 0.040 3 1895465 intergenic variant A/G;T snv 1
rs17162912 1.000 0.040 1 222801584 intergenic variant T/C snv 0.11 1
rs2097063 1.000 0.040 18 73963859 intron variant T/C snv 0.19 1
rs28696717 1.000 0.040 1 153493087 intergenic variant A/G snv 0.18 1
rs3933331 1.000 0.040 9 4389941 upstream gene variant G/C snv 0.23 1
rs4387163 1.000 0.040 1 165026476 intergenic variant G/A snv 0.44 1
rs4401971 1.000 0.040 9 11890045 intron variant A/C;G;T snv 1
rs4740788 1.000 0.040 9 4481668 intergenic variant T/C snv 0.16 1
rs6109227 1.000 0.040 20 12018497 intergenic variant A/T snv 0.79 1
rs6131293 1.000 0.040 20 12014779 intergenic variant A/G snv 0.79 1
rs6131295 1.000 0.040 20 12015619 regulatory region variant G/A;C snv 1
rs2364841
ADCK1
1.000 0.040 14 77817693 intron variant A/G snv 0.86 1
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs2071592
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.882 0.200 6 31547563 intron variant T/A;C snv 3
rs2883187
BDNF
1.000 0.040 11 27719545 5 prime UTR variant G/A snv 0.40 1
rs1519480
BDNF-AS
0.925 0.040 11 27654165 intron variant C/T snv 0.54 4