Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs3115667 0.882 0.200 6 31675622 downstream gene variant T/A;C snv 0.74 3
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 2
rs207186 0.925 0.120 1 55359252 intron variant C/T snv 7.7E-03 2
rs441399 1.000 0.120 15 90822992 regulatory region variant G/A snv 0.50 1
rs4934436 1.000 0.120 10 89023563 intergenic variant C/T snv 0.60 1
rs603097 1.000 0.120 18 54226736 upstream gene variant G/A snv 0.85 1
rs80202369 1.000 0.120 11 118873150 intergenic variant G/A snv 6.6E-03 1
rs2857597
AIF1
0.882 0.200 6 31617223 upstream gene variant T/A snv 0.74 3
rs61733010
AKR1A1
0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 2
rs150865017
ALDH1L1
1.000 0.120 3 126154627 missense variant G/A;T snv 1.6E-05; 4.0E-06 1
rs1127717
ALDH1L1-AS1 ; ALDH1L1
0.925 0.160 3 126107216 missense variant T/C snv 0.18 0.20 3
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1039312028
BAX
1.000 0.120 19 48955724 missense variant G/A snv 1.4E-05 1
rs1800477
BCL2
0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
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
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12