Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2883187
BDNF
1.000 0.040 11 27719545 5 prime UTR variant G/A snv 0.40 1
rs1148374
CDH2
1.000 0.040 18 28070318 intron variant T/A snv 0.31 1
rs12605662
CDH2
1.000 0.040 18 28171702 intron variant G/A snv 0.48 1
rs201333291
CDH2
1.000 0.040 18 27985092 missense variant T/C snv 4.0E-06 1.4E-05 1
rs4652867
DLGAP3
1.000 0.040 1 34901689 intron variant G/A;T snv 1
rs6662980
DLGAP3
1.000 0.040 1 34894477 intron variant A/G;T snv 1
rs7541937
DLGAP3
1.000 0.040 1 34876381 intron variant T/G snv 0.47 1
rs8190748
GAD2
1.000 0.040 10 26280826 intron variant A/G snv 0.44 1
rs1755715
GPR135
1.000 0.040 14 59440374 intron variant A/T snv 0.55 1
rs1417182
GRIK2
1.000 0.040 6 101885466 intron variant G/A snv 0.40 1