Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs186507655 0.708 0.280 1 1351675 upstream gene variant G/A snv 6.8E-03 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs2974935
MTX1
0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs73110464
KRT8
0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15