Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 1
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 14
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 5
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 3
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 2
rs2238126
ETV6
0.776 0.080 12 11856807 intron variant A/G snv 0.18 2
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 2
rs142319636
MMP2
0.790 0.080 16 55504828 intron variant A/G snv 3.7E-02 1
rs1424847607
EPHA2
1.000 0.080 1 16133591 missense variant A/G snv 4.0E-06 1
rs704017
ZMIZ1-AS1
0.776 0.080 10 79059375 intron variant A/G snv 0.55 1
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 1
rs7226855
SMAD7
0.790 0.080 18 48927678 intron variant A/G;T snv 1
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 31
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 2
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 2
rs9939049
CDH1
0.790 0.080 16 68778398 intron variant A/T snv 0.29 1
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 7
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 6