Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs34612342
MUTYH
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs763569821
MUC1
0.851 0.160 1 155188197 missense variant T/C snv 1.2E-05 4
rs3219472
TOE1 ; MUTYH
0.882 0.160 1 45338378 5 prime UTR variant C/T snv 0.26 3
rs3219476
MUTYH
0.882 0.200 1 45336998 intron variant A/C snv 0.58 3
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs9679162
GALNT14
0.882 0.120 2 31024648 intron variant G/T snv 0.48 4
rs1126580
CXCR2
0.882 0.120 2 218136243 3 prime UTR variant G/A;T snv 3
rs1194919682
CXCR4 ; LOC112268426
0.925 0.040 2 136115158 missense variant A/G snv 2
rs2230054
CXCR2
0.925 0.080 2 218135587 synonymous variant C/T snv 0.48 0.54 2
rs3769839
SP110 ; SP140
0.925 0.080 2 230211910 intron variant T/C snv 0.12 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs2289278
TSLP
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 5
rs7731017
DCTN4
0.925 0.080 5 150732056 intron variant T/C snv 8.3E-03 2
rs2076310
RXRB
0.925 0.080 6 33198257 intron variant A/G snv 0.27 0.28 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480