Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 43
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 41
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 41
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 40
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 36
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36