Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 8
rs4784227
CASC16
0.807 0.160 16 52565276 intron variant C/T snv 0.20 6
rs13283662
UHRF2
0.925 0.080 9 6428530 intron variant T/C snv 4
rs2306969
LOC101928844 ; FUT3
0.925 0.040 19 5851790 intron variant A/G snv 0.76 4
rs17506395
TP63
0.925 0.080 3 189803530 intron variant T/G snv 0.19 3
rs2787486
STXBP4
0.925 0.080 17 55132413 intron variant A/C snv 0.33 3
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 4
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 9
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 7
rs80357086
BRCA1
0.851 0.200 17 43106480 stop gained A/G;T snv 5
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 2
rs62625308
BRCA1
0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 2
rs80358920
BRCA2
0.732 0.400 13 32346841 stop gained C/G;T snv 2
rs273898674
BRCA1
0.925 0.200 17 43093472 stop gained G/A snv 1
rs397507828
BRCA2
1.000 13 32340440 stop gained G/T snv 1
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 1
rs80356923
BRCA1
0.882 0.200 17 43091891 stop gained C/A;T snv 9.9E-05 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 83