Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1075650
IER5L
9 129176634 3 prime UTR variant T/C snv 0.25 1
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs11503014
GABRA2
1.000 0.080 4 46388848 5 prime UTR variant C/G snv 0.27 2
rs12043259
NFASC
1 204858913 intron variant C/G snv 0.11 2
rs1212415280
VEGFA
6 43771130 missense variant G/T snv 2.1E-05 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1409568 1.000 0.040 10 118871273 intron variant T/C snv 8.2E-02 2
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1611131
DBH-AS1 ; DBH
0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 3
rs16918875
OPRK1
8 53229594 synonymous variant G/A snv 4.3E-02 7.1E-02 1
rs17228602
ACHE ; UFSP1
7 100890786 3 prime UTR variant C/T snv 1.5E-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
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1803274
BCHE
0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1875999
CRHBP
5 76969157 3 prime UTR variant T/C snv 0.38 1
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2070762
TH
0.925 0.080 11 2165105 intron variant A/G snv 0.43 5