Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs12883384
MDGA2
1.000 0.040 14 46934481 intron variant A/C;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs9561329
GPC6
1.000 0.040 13 93358916 intron variant A/G snv 0.15 2
rs1010657
TACC2
1.000 0.040 10 122238202 intron variant A/G snv 0.35 1
rs1317926854
TPH2
1.000 0.040 12 72031625 missense variant A/G snv 1
rs883473
CHRNA7
1.000 0.040 15 32033473 intron variant A/G snv 0.57 1
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs8015351 1.000 0.040 14 49421667 intergenic variant A/G;T snv 1
rs1490265
SUCLG2
1.000 0.040 3 67401619 intron variant C/A snv 0.74 2
rs3756242
CD38
1.000 0.040 4 15784379 intron variant C/A snv 0.15 1
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 7
rs4965121 1.000 0.040 15 97975562 downstream gene variant C/A;G snv 2
rs628604 1.000 0.040 19 54028370 upstream gene variant C/A;G;T snv 1
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs2835731
DYRK1A
1.000 0.040 21 37424426 intron variant C/G;T snv 0.17 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2337980
CHRNA7
0.925 0.120 15 32151995 intron variant C/T snv 0.45 2
rs9491140
NKAIN2
1.000 0.040 6 124370091 intron variant C/T snv 0.39 2
rs12537271
APTR ; LOC105375363
1.000 0.040 7 77671409 intron variant C/T snv 0.36 1
rs13104011
CD38
1.000 0.040 4 15805410 intron variant C/T snv 0.15 1
rs6495307
CHRNA3
1.000 0.040 15 78597979 intron variant C/T snv 0.39 1
rs912765 1.000 0.040 1 87178264 intergenic variant C/T snv 0.45 1