Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs10937921 1.000 0.120 4 3274764 downstream gene variant C/T snv 0.40 2
rs1138690 1.000 0.120 4 3289674 upstream gene variant G/A;T snv 1
rs12668183 1.000 0.120 7 16455781 regulatory region variant T/C snv 0.34 1
rs7658462 1.000 0.120 4 3281695 intergenic variant C/T snv 0.16 1
rs1277892620
ACACA
0.925 0.120 17 37242036 synonymous variant A/G snv 4.0E-06 7.0E-06 2
rs762847
ADD1
1.000 0.120 4 2910336 intron variant A/G snv 0.54 1
rs73786719
ADGB
1.000 0.120 6 146716848 intron variant C/A snv 1.7E-02 3.3E-02 1
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2292779
AGO2
0.851 0.320 8 140551294 intron variant G/C;T snv 0.57; 4.9E-06 4
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs36117895
ATG7
1.000 0.120 3 11358545 missense variant T/C snv 3.2E-02 3.9E-02 1
rs1382597320
ATN1
0.882 0.160 12 6934305 missense variant A/G snv 7.0E-06 3
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1170668763
BECN1
1.000 0.120 17 42818395 missense variant T/A snv 7.0E-06 1
rs756573441
CALD1
1.000 0.120 7 134933359 missense variant A/G;T snv 4.2E-06 1
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs644236
DROSHA
0.882 0.320 5 31409008 non coding transcript exon variant T/C snv 0.31 0.35 5