Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs912765 1.000 0.040 1 87178264 intergenic variant C/T snv 0.45 1
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1490265
SUCLG2
1.000 0.040 3 67401619 intron variant C/A snv 0.74 2
rs2270463
SSUH2 ; CAV3
1.000 0.040 3 8733391 intron variant G/T snv 0.23 1
rs709160
TSEN2
1.000 0.040 3 12484903 intron variant G/C snv 0.56 1
rs13104011
CD38
1.000 0.040 4 15805410 intron variant C/T snv 0.15 1
rs3756242
CD38
1.000 0.040 4 15784379 intron variant C/A snv 0.15 1
rs6832769
CLOCK ; TMEM165
1.000 0.040 4 55432027 3 prime UTR variant G/A snv 0.68 1
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs9491140
NKAIN2
1.000 0.040 6 124370091 intron variant C/T snv 0.39 2
rs111339162
OPRM1
1.000 0.040 6 154039596 missense variant G/A snv 2.0E-05 1.4E-04 1
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
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
rs2267717
CRHR2
1.000 0.040 7 30677427 intron variant G/A snv 0.17 1
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs2609997
LOC101929415 ; PENK
0.882 0.120 8 56447926 intron variant T/C snv 0.34 3
rs2576573
LOC101929415 ; PENK
0.925 0.120 8 56445416 3 prime UTR variant G/A snv 0.38 2
rs16921695
LINC01606
1.000 0.040 8 57145096 intron variant T/G snv 0.33 1
rs1010657
TACC2
1.000 0.040 10 122238202 intron variant A/G snv 0.35 1
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
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs208294
P2RX7 ; LOC105370032
0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9