Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs6713088
ACYP2
0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs843711
ACYP2
0.790 0.200 2 54251980 intron variant C/T snv 0.41 7
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs843706
ACYP2 ; TSPYL6
0.807 0.160 2 54253232 3 prime UTR variant C/A snv 0.42 6
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs12732894
ARHGEF10L
0.882 0.080 1 17582733 intron variant G/A snv 1.6E-02 3
rs2244444
ARHGEF10L
0.882 0.080 1 17520426 intergenic variant C/T snv 0.55 3
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1330010954
DLC1
0.882 0.080 8 13094897 missense variant C/T snv 4.0E-06 4
rs372894000
DLC1
0.882 0.080 8 13092766 missense variant C/T snv 2.0E-05 1.4E-05 4
rs756966085
DLC1
0.882 0.080 8 13090431 missense variant C/T snv 8.0E-06 7.0E-06 4
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs5854292
EGFEM1P
0.851 0.080 3 168680960 intron variant AA/-;A;AAA delins 5
rs3212948
ERCC1
0.776 0.160 19 45421104 intron variant G/C snv 0.53 10