Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs140701
SLC6A4
0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs1418688 1.000 0.040 6 71169166 downstream gene variant A/G;T snv 1
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs1487275
TPH2
1.000 0.040 12 72016512 intron variant C/A snv 0.71 1
rs16938184
PRDM11
1.000 0.040 11 45179068 intron variant G/A;C snv 1
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs17260539 1.000 0.040 9 12182545 intergenic variant G/A snv 6.6E-02 1
rs173365
MAPT-AS1 ; LINC02210-CRHR1 ; CRHR1
0.882 0.080 17 45823708 intron variant A/G snv 0.55 3
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs1800857
CCKAR
0.851 0.120 4 26489489 splice region variant A/G snv 0.17 0.18 4
rs1805067
SLC6A2
0.925 0.080 16 55698511 missense variant G/A snv 2.8E-05 2.1E-05 2
rs1819741 1.000 0.040 1 192815708 intron variant T/A;C snv 1
rs191260602
GLRB
1.000 0.040 4 157140489 intron variant A/G snv 7.7E-03 1
rs2039391
FOCAD
1.000 0.040 9 20714015 intron variant C/T snv 0.86 1
rs2241165
GAD1
1.000 0.040 2 170821869 non coding transcript exon variant C/T snv 0.63 1
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs2296972
HTR2A-AS1 ; HTR2A
0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs242924
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.882 0.080 17 45808001 intron variant G/T snv 0.44 3