Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 9
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs3796863
CD38
0.790 0.160 4 15848363 intron variant G/T snv 0.41 8
rs769236847
CZ1P-ASNS ; ASNS
0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 8
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs1800561
CD38
0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 7
rs6782011
GRM7
0.807 0.120 3 7457960 intron variant C/T snv 0.52 7
rs6323
MAOA
0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs1799836
MAOB
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7
rs344781
PLAUR
0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7
rs1390938
SLC18A1
0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs301430
SLC1A1 ; SPATA6L
0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs878853161
SLC2A1
0.851 0.240 1 42929977 frameshift variant AT/- del 7
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 7
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs7794745
CNTNAP2
0.851 0.040 7 146792514 intron variant A/T snv 0.49 6
rs2070011
FGA
0.807 0.120 4 154590745 5 prime UTR variant T/A;C snv 6
rs797045050
KIF1A
0.807 0.120 2 240797715 missense variant C/T snv 6
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6