Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7123390
CRY2
0.882 0.160 11 45869867 intron variant G/A snv 0.22 0.22 3
rs6948
CASP3
1.000 0.120 4 184627976 3 prime UTR variant G/T snv 0.48 3
rs6736233
CASP8
1.000 0.120 2 201254251 intron variant G/C snv 0.16 1
rs6467
CYP21A2
0.925 0.320 6 32039081 missense variant C/A;G;T snv 0.64; 2.3E-03 3
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs61733010
AKR1A1
0.925 0.120 1 45561805 missense variant C/G;T snv 4.0E-06; 4.3E-04 1.9E-03 2
rs606231364
FAS
0.925 0.160 10 89003071 missense variant G/A snv 2
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs603097 1.000 0.120 18 54226736 upstream gene variant G/A snv 0.85 1
rs6002551
CENPM
1.000 0.120 22 41942148 intron variant G/A snv 0.20 1
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs56287471
LOC107986469 ; IL12B
1.000 0.120 5 159323135 missense variant C/T snv 3.8E-04 1.5E-03 1
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs4934436 1.000 0.120 10 89023563 intergenic variant C/T snv 0.60 1
rs4901706
TMEM260
1.000 0.120 14 56647667 3 prime UTR variant G/A;C;T snv 3
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 5
rs4661636
CASP9
0.925 0.160 1 15496566 intron variant C/T snv 0.24 2
rs4648022
NFKB1
1.000 0.120 4 102575280 intron variant C/A;T snv 1
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10