Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045433
TRNT1 ; CRBN
1.000 0.160 3 3149742 non coding transcript exon variant T/C snv 0.15 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 8
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 22
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
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 2
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 1
rs1049623
DDR1
0.925 0.200 6 30897052 synonymous variant T/C snv 0.47 0.43 2
rs1049633
DDR1
1.000 0.160 6 30899750 3 prime UTR variant G/A snv 7.6E-02 1
rs1052501
ULK4
0.925 0.160 3 41883906 missense variant C/G;T snv 0.80 2
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 1
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 3
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 4
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs10936602
LRRIQ4
0.882 0.240 3 169818849 upstream gene variant T/C snv 0.26 2
rs11064392
CD4
1.000 0.160 12 6789226 intron variant A/G snv 0.14 1
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 22