Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 6
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 4
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs12512631 0.882 0.200 4 71735614 intergenic variant T/C snv 0.35 3
rs4911414 0.882 0.120 20 34141638 regulatory region variant T/G snv 0.73 2
rs1015362 0.925 0.080 20 34150806 regulatory region variant C/T snv 0.42 1
rs1015363 1.000 0.040 20 34150529 intergenic variant G/A snv 0.69 1
rs10816595 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 1
rs2127675 1.000 0.040 6 32883073 upstream gene variant A/G snv 0.36 1
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 1
rs6673928 1.000 0.040 1 206763900 downstream gene variant G/T snv 0.20 1
rs6695772 1.000 0.040 1 212708597 intergenic variant C/G snv 0.58 1
rs1351212535
ABCA1
1.000 0.040 9 104831015 missense variant T/A snv 4.0E-06 1
rs10231520
ABCB5
1.000 0.040 7 20742471 intron variant C/T snv 0.29 1
rs17817117
ABCB5
1.000 0.040 7 20685203 intron variant G/C snv 0.29 1
rs2301641
ABCB5
1.000 0.040 7 20658647 missense variant A/G snv 0.33 0.40 1
rs749499406
ACD
1.000 0.040 16 67658771 missense variant C/T snv 4.0E-06 1
rs1800522
AIRE
1.000 0.040 21 44297667 synonymous variant T/C snv 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1057519804
AKT1
1.000 0.040 14 104776711 missense variant G/T snv 1
rs397514644
AKT1
0.925 0.040 14 104780190 missense variant G/A snv 7.0E-06 1
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 13
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 13
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs137854567
APC
0.882 0.120 5 112819272 missense variant C/A;G;T snv 4.0E-06; 6.7E-04 1