Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs344781
PLAUR
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs6782011
GRM7
0.807 0.120 3 7457960 intron variant C/T snv 0.52 7
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 7
rs878853161
SLC2A1
0.851 0.240 1 42929977 frameshift variant AT/- del 7
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs16835979
STX18-AS1
0.851 0.120 4 4633549 intron variant C/A snv 0.20 6
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs1843809
TPH2
0.851 0.080 12 71954918 intron variant G/T snv 0.77 6
rs2070011
FGA
0.807 0.120 4 154590745 5 prime UTR variant T/A;C snv 6
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs2745557
PACERR ; PTGS2
0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs4774388
RORA
0.807 0.200 15 61174799 intron variant C/T snv 0.81 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs6824295
STX18-AS1
0.851 0.120 4 4612553 intron variant C/T snv 0.20 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs797045050
KIF1A
0.807 0.120 2 240797715 missense variant C/T snv 6
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs167771
DRD3
0.827 0.280 3 114157428 intron variant G/A;T snv 5
rs2279357
CYP11A1
0.851 0.160 15 74338282 intron variant T/C snv 0.69 5