Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79658334
RET
0.662 0.360 10 43119548 missense variant G/A;C;T snv 1.2E-04; 4.3E-06 21
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 17
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 16
rs75996173
RET
0.716 0.240 10 43114501 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 16
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 12
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs3741219
MRPL23 ; H19 ; HOTS
0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 9
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs387906698
PRSS1
0.827 0.040 7 142751919 missense variant C/A;T snv 4.0E-06; 7.2E-05 8
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs763538721
HIF1A-AS3 ; HIF1A
0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8
rs12918952
WWOX
0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 7
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs3130
PROM1 ; FGFBP2
0.882 0.080 4 15968315 3 prime UTR variant T/A;C snv 6
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs80358829
BRCA2
0.827 0.120 13 32340327 missense variant C/T snv 6
rs104894403
GJB2
0.851 0.240 13 20189386 missense variant C/A;G;T snv 4.0E-06 5
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 5
rs121918461
PTPN11
0.827 0.240 12 112450362 missense variant A/C;G;T snv 5
rs1329032366
PDLIM5
0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5