Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 1
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 1
rs16941835 0.790 0.080 16 86662114 intron variant G/C snv 0.20 1
rs2423279 0.790 0.080 20 7831703 downstream gene variant T/C snv 0.29 1
rs6061231 0.790 0.080 20 62381861 downstream gene variant C/A snv 0.28 1
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 1
rs72647484 0.790 0.080 1 22261235 regulatory region variant T/C snv 6.2E-02 1
rs964293 0.790 0.080 20 54200178 TF binding site variant C/A;T snv 1
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 1
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 1
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 1
rs2427308
CABLES2
0.790 0.080 20 62394395 intron variant C/T snv 0.22 1
rs10774214
CCND2-AS1
0.790 0.080 12 4259186 intron variant T/C snv 0.54 1
rs9939049
CDH1
0.790 0.080 16 68778398 intron variant A/T snv 0.29 1
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 1
rs209489
ELOVL5
0.790 0.080 6 53312880 intron variant C/A snv 0.92 1
rs7252505
GPATCH1
0.790 0.080 19 33084158 intron variant G/A snv 0.29 1
rs5934683
GPR143
0.790 0.080 X 9783434 intron variant T/C snv 0.50 1
rs17094983
LINC01500
0.776 0.080 14 58722643 intron variant G/A snv 0.12 1
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 1
rs2450115
LOC105375712
0.790 0.080 8 116611854 intergenic variant T/C snv 0.19 1
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 1
rs7528276
MACF1
0.790 0.080 1 39344315 intron variant T/A;C snv 1
rs63750781
MLH1
0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1
rs142319636
MMP2
0.790 0.080 16 55504828 intron variant A/G snv 3.7E-02 1