Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs2020936
SLC6A4
0.776 0.160 17 30223796 intron variant G/A;C snv 10
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 7
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs680244
CHRNA5
0.882 0.120 15 78578946 intron variant T/C snv 0.60 4
rs2609997
LOC101929415 ; PENK
0.882 0.120 8 56447926 intron variant T/C snv 0.34 3
rs12883384
MDGA2
1.000 0.040 14 46934481 intron variant A/C;T snv 2
rs1490265
SUCLG2
1.000 0.040 3 67401619 intron variant C/A snv 0.74 2
rs1909884
CHRNA7
0.925 0.120 15 32147097 intron variant G/A snv 0.41 2
rs2337980
CHRNA7
0.925 0.120 15 32151995 intron variant C/T snv 0.45 2
rs2835731
DYRK1A
1.000 0.040 21 37424426 intron variant C/G;T snv 0.17 2
rs9491140
NKAIN2
1.000 0.040 6 124370091 intron variant C/T snv 0.39 2
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
rs10251794
CNTNAP2
1.000 0.040 7 146988457 intron variant T/A snv 0.26 1
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
rs16921695
LINC01606
1.000 0.040 8 57145096 intron variant T/G snv 0.33 1
rs2267717
CRHR2
1.000 0.040 7 30677427 intron variant G/A snv 0.17 1
rs2270463
SSUH2 ; CAV3
1.000 0.040 3 8733391 intron variant G/T snv 0.23 1
rs362584
SNAP25-AS1 ; SNAP25
1.000 0.040 20 10273827 intron variant G/A snv 0.24 1
rs3756242
CD38
1.000 0.040 4 15784379 intron variant C/A snv 0.15 1
rs555018
CHRNA5
1.000 0.040 15 78586900 intron variant G/A snv 0.64 1
rs601079
CHRNA5
1.000 0.040 15 78577237 intron variant T/A;G snv 1