Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7651446
TIPARP
0.882 0.120 3 156689208 intron variant G/T snv 7.9E-02 3
rs4648551
TP73
0.882 0.120 1 3716166 intron variant G/A snv 0.32 3
rs6695978
TP73
0.882 0.120 1 3731781 intron variant G/A snv 7.3E-02 3
rs2287497
WRAP53 ; TP53
0.882 0.120 17 7689462 intron variant G/A snv 0.25 3
rs587780128
XRCC2
0.882 0.160 7 152649010 missense variant G/A snv 1.2E-05 3.5E-05 3
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs7313833 0.851 0.120 12 27930263 intergenic variant G/A snv 0.37 4
rs74315464
ARSA
0.882 0.120 22 50627048 missense variant G/A;C snv 4
rs1801243
ATP7B
0.851 0.200 13 51974004 missense variant A/C;T snv 0.44; 2.0E-05 4
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs80357233
BRCA1
0.882 0.200 17 43093393 stop gained G/C;T snv 4.0E-06 4
rs876660702
BRCA1
0.851 0.160 17 43063333 splice region variant C/T snv 4
rs4987046
BRCA2
0.925 0.160 13 32319134 missense variant A/G snv 1.6E-03 1.6E-03 4
rs4988344
BRIP1
0.882 0.120 17 61847251 intron variant G/C snv 0.20 0.15 4
rs6886
CAPG
0.925 0.160 2 85394936 missense variant T/A;C snv 0.58 4
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 4
rs1444192401
KRT7
0.882 0.120 12 52235347 missense variant G/A snv 4
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs2073495
LTF
0.851 0.200 3 46439467 missense variant C/A;G snv 4.9E-04; 0.33 4
rs9110
LTF
0.851 0.200 3 46439310 missense variant A/C;G;T snv 0.39 0.40 4
rs230521
NFKB1
0.851 0.160 4 102542171 intron variant C/G snv 0.59 4
rs6443626
PIK3CA ; KCNMB3
0.851 0.200 3 179237995 3 prime UTR variant T/C snv 0.24 4