Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs751416416
OPRK1
0.882 0.120 8 53250920 missense variant C/A;T snv 8.3E-06; 4.1E-06 5
rs774847933
COMT ; MIR4761
0.882 0.200 22 19962797 missense variant A/G snv 8.0E-06 5
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs702764
OPRK1
0.925 0.120 8 53229597 synonymous variant T/C;G snv 0.17; 8.0E-06 4
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs3495
BCHE
0.925 0.160 3 165773193 3 prime UTR variant C/A;T snv 3
rs772527880
AGFG1
2 227531108 missense variant G/A snv 4.0E-06 1
rs75012854
MIR4761 ; COMT
0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs764987358
ANGPT1
1.000 0.160 8 107347040 missense variant C/A snv 8.0E-06 1.4E-05 2
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-02 2
rs2377339
NCK2
2 105840835 intron variant A/G snv 4.8E-02 2
rs16918875
OPRK1
8 53229594 synonymous variant G/A snv 4.3E-02 7.1E-02 1
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs17228616
ACHE ; UFSP1
1.000 0.080 7 100890100 3 prime UTR variant G/T snv 9.8E-02 3
rs17664708
NRG1
1.000 0.080 8 32579499 intron variant C/T snv 1.0E-01 2
rs12043259
NFASC
1 204858913 intron variant C/G snv 0.11 2
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95