Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs9363918 0.882 0.200 6 68432116 intron variant T/G snv 0.38 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs34301344
ARL11
0.689 0.400 13 49630893 stop gained G/A snv 9.7E-03 7.9E-03 22
rs1864183
ATG10
0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs80359601
BRCA2
0.807 0.360 13 32340890 frameshift variant -/A;NNNNNNNN ins 4.1E-06 8
rs748148861
CCR6
0.925 0.120 6 167136856 missense variant G/C snv 8.0E-06 2
rs5744455
CD14 ; TMCO6
0.882 0.160 5 140633722 upstream gene variant G/A;T snv 5
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs142863665
CUX1
1.000 0.120 7 102111708 missense variant G/A snv 3.2E-05 1.3E-04 1
rs771176824
CUX1
1.000 0.120 7 101916181 missense variant C/A;T snv 1
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs13078
DICER1
0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs6877842
DROSHA ; C5orf22
0.807 0.320 5 31532531 intron variant G/C snv 0.16 7
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs4253211
ERCC6
0.882 0.240 10 49470271 missense variant C/G;T snv 7.1E-02; 2.0E-05 3
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12