Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6678517
LAMC1
0.776 0.080 1 183033504 intron variant A/G;T snv 10
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs12143541
TTC22
0.790 0.080 1 54782179 intron variant A/G snv 0.11 9
rs201395236
EFCAB2
0.790 0.080 1 245018119 intron variant T/C snv 1.5E-04 9
rs2184857
LOC105373224
0.790 0.080 1 239918447 upstream gene variant A/C snv 0.45 9
rs3753366
GNG12
0.790 0.080 1 67729450 intron variant C/G snv 0.20 9
rs4546885
LAMC1
0.790 0.080 1 183056420 intron variant G/A;C snv 9
rs658191
MACF1
0.790 0.080 1 39458103 non coding transcript exon variant C/G snv 6.1E-02 9
rs6658977 0.790 0.080 1 221876478 downstream gene variant G/T snv 0.29 9
rs6691195 0.790 0.080 1 221989031 downstream gene variant C/A snv 0.19 9
rs67376798
DPYD
0.851 0.120 1 97082391 missense variant T/A snv 2.8E-03 3.3E-03 9
rs72647484 0.790 0.080 1 22261235 regulatory region variant T/C snv 6.2E-02 9
rs7528276
MACF1
0.790 0.080 1 39344315 intron variant T/A;C snv 9
rs7542665
L1TD1
0.790 0.080 1 62207365 missense variant T/C snv 0.63 0.67 9
rs5273
PTGS2
0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs3093075 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 5
rs35301225
MIR34A ; MIR34AHG
0.882 0.080 1 9151743 mature miRNA variant C/A;T snv 5
rs3219145
PARP1
0.882 0.120 1 226363128 missense variant T/C;G snv 1.2E-02; 4.0E-06 4
rs6588147
LEPR
0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
rs6598964
LIN28A
0.882 0.080 1 26419836 intron variant A/G snv 0.67 3
rs730881834
MUTYH
0.882 0.120 1 45332181 missense variant G/C snv 3
rs374400
OBSCN
0.925 0.080 1 228347383 intron variant C/T snv 0.40 2
rs4548444
MAPKAPK2
0.925 0.080 1 206716793 intron variant A/G snv 0.20 2
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38