Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912665
TP53
1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs771386507
HLA-B ; MIR6891
0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs1456079929
PGR
0.851 0.120 11 101042001 missense variant C/A snv 8.0E-06 5
rs540432391
CGB5
0.882 0.120 19 49043993 5 prime UTR variant G/A;C snv 5
rs7246045
CGB5
0.882 0.120 19 49042825 upstream gene variant T/G snv 2.9E-02 5
rs755378873
SLC13A5
0.851 0.120 17 6694197 missense variant C/A;T snv 4.0E-06 5
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
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs1444192401
KRT7
0.882 0.120 12 52235347 missense variant G/A snv 4
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs2072590
HAGLR ; HAGLROS
0.851 0.120 2 176177905 non coding transcript exon variant A/C;T snv 4
rs2287498
WRAP53 ; TP53
0.882 0.120 17 7689242 synonymous variant C/T snv 0.13 0.14 4
rs4988344
BRIP1
0.882 0.120 17 61847251 intron variant G/C snv 0.20 0.15 4
rs587780259
RAD51C
0.882 0.120 17 58709857 splice acceptor variant A/C;G snv 2.0E-05 2.1E-05 4
rs67164370
RASSF2
0.851 0.120 20 4787830 intron variant -/AGGGACT ins 4
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
rs10098821
LINC00824
0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 3
rs1064793881
TP53
0.925 0.120 17 7673784 missense variant C/T snv 3
rs10962692 0.925 0.120 9 16915876 upstream gene variant G/A;C snv 3