Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2835731
DYRK1A
1.000 0.040 21 37424426 intron variant C/G;T snv 0.17 2
rs4965121 1.000 0.040 15 97975562 downstream gene variant C/A;G snv 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
rs1055356
AQR
1.000 0.040 15 34855901 3 prime UTR variant T/C snv 0.42 1
rs111339162
OPRM1
1.000 0.040 6 154039596 missense variant G/A snv 2.0E-05 1.4E-04 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
rs1317926854
TPH2
1.000 0.040 12 72031625 missense variant A/G snv 1
rs1434789
DEFB127
1.000 0.040 20 157259 upstream gene variant T/G snv 0.29 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
rs2770378
LOC101929098 ; OXT
1.000 0.040 20 3072868 downstream gene variant G/A snv 0.38 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
rs628604 1.000 0.040 19 54028370 upstream gene variant C/A;G;T snv 1
rs6495307
CHRNA3
1.000 0.040 15 78597979 intron variant C/T snv 0.39 1
rs6832769
CLOCK ; TMEM165
1.000 0.040 4 55432027 3 prime UTR variant G/A snv 0.68 1