Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 40
rs1029044314
DDR1
0.851 0.040 6 30898095 missense variant G/A snv 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 2
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 43
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 58
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 23
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs1057519902
H3-3A
0.742 0.160 1 226064451 missense variant G/C snv 13
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 26
rs1057519904
H3C11
0.742 0.080 6 27872233 missense variant T/A snv 14
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 1
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 1
rs1057519945
POLE
0.776 0.200 12 132673703 missense variant C/A;T snv 7
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 2
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 9
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 1
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 1
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 3
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 1
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 4