Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2123926
LYSMD4
1.000 0.040 15 99724313 intron variant T/C snv 0.19 2
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs531564
LINC00599 ; MIR124-1
0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs10760580 1.000 0.040 9 98899368 TF binding site variant G/A snv 0.22 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs55884448
MMS22L
1.000 0.040 6 97153651 intron variant G/A snv 1.0E-02 2
rs73758118
KLHL32
1.000 0.040 6 97131188 intron variant T/A snv 9.7E-03 3
rs73758117
KLHL32
1.000 0.040 6 97125724 intron variant C/T snv 9.7E-03 2
rs73758115
KLHL32
1.000 0.040 6 97123820 intron variant C/T snv 9.7E-03 2
rs60451608
KLHL32
1.000 0.040 6 97108568 intron variant T/G snv 9.8E-03 2
rs13382275
SNTG2
1.000 0.040 2 969893 intron variant A/G snv 0.12 2
rs145174011
HAL
1.000 0.040 12 95984922 intron variant T/A snv 4.9E-03 1
rs7307510
LOC105369921
1.000 0.040 12 95843792 intron variant T/C snv 0.80 1
rs153916
SPATA9
1.000 0.040 5 95700996 upstream gene variant C/A;G;T snv 4
rs17264034 0.925 0.080 5 9557490 regulatory region variant G/A snv 0.13 2
rs3735590
PON1
0.925 0.080 7 95298183 3 prime UTR variant G/A snv 0.14 3
rs60129850
FGD6
1.000 0.040 12 95144245 intron variant C/A snv 0.20 1
rs4762172
FGD6 ; LOC112268099
1.000 0.040 12 95100136 intron variant T/C snv 0.13 1
rs1800463
SERPINA3
1.000 0.040 14 94614674 missense variant T/A;C snv 2
rs8004738
SERPINA1
0.925 0.080 14 94390577 5 prime UTR variant G/A snv 0.55 2
rs1243160
SERPINA1
1.000 0.040 14 94388540 intron variant G/A snv 0.16 1
rs2854254
SERPINA1
1.000 0.040 14 94388536 intron variant T/C snv 0.64 1
rs1555369299
SERPINA1
0.882 0.160 14 94383237 start lost T/- delins 3
rs1457464431
SERPINA1
0.882 0.160 14 94383069 missense variant A/G snv 3
rs28931570
SERPINA1
0.882 0.160 14 94383051 missense variant G/A snv 1.1E-03 1.5E-03 3