Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs1126579
CXCR2
0.776 0.200 2 218136011 3 prime UTR variant T/C snv 0.62 8
rs2289278
TSLP
0.827 0.200 5 111073450 5 prime UTR variant C/G snv 8.7E-02 5
rs11635252
CRTC3
0.925 0.080 15 90528542 upstream gene variant T/C snv 0.88 4
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
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
rs1194919682
CXCR4 ; LOC112268426
0.925 0.040 2 136115158 missense variant A/G snv 2
rs3769839
SP110 ; SP140
0.925 0.080 2 230211910 intron variant T/C snv 0.12 2
rs7731017
DCTN4
0.925 0.080 5 150732056 intron variant T/C snv 8.3E-03 2
rs8004738
SERPINA1
0.925 0.080 14 94390577 5 prime UTR variant G/A snv 0.55 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1003723
LDLR ; MIR6886
0.925 0.080 19 11113505 non coding transcript exon variant C/A;T snv 4.0E-06; 0.40 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193