Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs1114167293
C12orf57
0.807 0.320 12 6944474 splice acceptor variant A/G snv 4.0E-06 7
rs1564691414
FAS
0.925 0.160 10 89007698 splice acceptor variant A/G snv 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs373611092
MIR4761 ; COMT
0.925 0.160 22 19962794 missense variant A/G snv 8.4E-05 4.9E-05 5
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs4969239
BAIAP2
0.882 0.120 17 81036744 intron variant A/G snv 0.11 3
rs740603
COMT
0.925 0.040 22 19957654 intron variant A/G snv 0.48 3
rs1057517991
MC4R
0.925 0.120 18 60371539 missense variant A/G snv 4.0E-06 2
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs1170695
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11013652 5 prime UTR variant A/G snv 0.35 2
rs145108385
LOC648987
0.925 0.040 5 43054645 intron variant A/G snv 2
rs2228607
STX1A
0.925 0.160 7 73708593 synonymous variant A/G snv 0.51 0.53 2
rs2652511
SLC6A3
0.925 0.040 5 1446274 upstream gene variant A/G snv 0.51 2