Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7163702 0.925 0.080 15 28460135 upstream gene variant C/A snv 2
rs722025 0.925 0.080 5 8107899 intergenic variant A/G snv 0.27 2
rs823920 0.925 0.080 9 101900303 intergenic variant A/G snv 0.12 2
rs11568591
ABCC3
0.925 0.080 17 50683692 missense variant G/A snv 3.7E-02 3.9E-02 2
rs1367801477
ACD ; CARMIL2
0.925 0.080 16 67657673 missense variant T/C snv 4.0E-06 2
rs754141936
AGER
0.925 0.080 6 32182641 missense variant G/C snv 4.1E-06 1.4E-05 2
rs900321363
AGER
0.925 0.080 6 32183616 synonymous variant C/T snv 2.1E-05 2
rs2229995
APC
0.925 0.080 5 112843098 missense variant G/A snv 2.0E-02 1.7E-02 2
rs530670052
APC
0.925 0.080 5 112801313 missense variant A/G snv 1.6E-05 1.4E-05 2
rs79896135
APC
0.925 0.080 5 112707585 5 prime UTR variant C/A;G;T snv 2
rs35514263
ATR
0.925 0.080 3 142579202 upstream gene variant C/G;T snv 2
rs2284396
BCL2L14 ; LRP6
0.925 0.080 12 12122001 intron variant T/C snv 0.45 2
rs3808348
C7orf50 ; CYP2W1
0.925 0.080 7 988812 missense variant C/T snv 0.21 0.17 2
rs149418249
CARMIL2 ; ACD
0.925 0.080 16 67657798 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs492510
CHEK1
0.925 0.080 11 125627447 intron variant A/G;T snv 2
rs5762748
CHEK2
0.925 0.080 22 28694902 intron variant G/A snv 6.3E-02 2
rs11704
CINP ; ZNF839
0.925 0.080 14 102342318 3 prime UTR variant G/C snv 0.26 2
rs13072632
CTNNB1
0.925 0.080 3 41220953 5 prime UTR variant T/C snv 0.41 2
rs1902584
CYP19A1 ; LOC112268146
0.925 0.080 15 51319457 intron variant A/T snv 8.2E-02 2
rs1376199019
CYP1A1
0.925 0.080 15 74720557 missense variant T/C snv 4.0E-06 2
rs1329149
CYP2E1
0.925 0.080 10 133536297 intron variant T/C snv 0.73 2
rs6485350
DKK3
0.925 0.080 11 11992070 intron variant G/A snv 0.56 2
rs1419316960
DNMT1
0.925 0.080 19 10166651 missense variant T/C snv 7.0E-06 2
rs1282801317
EGFR
0.925 0.080 7 55143316 missense variant G/C snv 4.0E-06 2
rs1330586270
EPHB2
0.925 0.080 1 22882367 missense variant G/A snv 2