Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11111 0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs13440581 0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 5
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2072115 0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs228697 0.882 0.080 1 7827519 missense variant C/G snv 8.7E-02 7.3E-02 5
rs3096140 0.882 0.080 5 37832731 intron variant G/A snv 0.69 5
rs2349775 0.851 0.120 7 8678450 intron variant G/A;C snv 6
rs41305272 0.851 0.120 15 67807105 3 prime UTR variant C/T snv 2.4E-02 6
rs1202184 0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs2072621 0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs2740210 0.827 0.120 20 3072609 downstream gene variant C/A snv 0.28 7
rs57875989 0.882 0.080 1 7829913 splice acceptor variant GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC delins 0.11 0.18 7
rs7194256 0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs1922242 0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs1881457 0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs2020936 0.776 0.160 17 30223796 intron variant G/A;C snv 10
rs2298383 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs3213207 0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs6354 0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16