Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1143684
NQO2
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84 4
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467
HIF1A ; HIF1A-AS3
0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11554495
KRT8
0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 16
rs11571836
BRCA2
0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs11644322
WWOX
0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs11655237
LINC00511 ; LINC00673
0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs1176026649
CBR4 ; PALLD
0.851 0.120 4 168921582 missense variant C/T snv 7.2E-06 4
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1209809979
AKR1A1
0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913527
KRAS
0.807 0.320 12 25225628 missense variant C/A;G;T snv 6
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 55