Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs2079742 | 0.851 | 0.240 | 17 | 61388336 | non coding transcript exon variant | T/C | snv | 0.20 | 7 | ||
rs1544935 | 0.925 | 0.160 | 6 | 39156672 | intergenic variant | T/G | snv | 0.18 | 3 | ||
rs11746443 | 0.882 | 0.120 | 5 | 177371305 | intron variant | G/A | snv | 0.24 | 0.21 | 3 | |
rs6123359 | 1.000 | 0.080 | 20 | 54098167 | regulatory region variant | A/G | snv | 0.12 | 2 | ||
rs7277076 | 1.000 | 0.080 | 21 | 36464675 | intron variant | T/C | snv | 0.52 | 2 | ||
rs2286526 | 1.000 | 0.080 | 17 | 61394696 | non coding transcript exon variant | C/G;T | snv | 2 | |||
rs3798519 | 1.000 | 0.080 | 6 | 50821065 | intron variant | A/C;G | snv | 2 | |||
rs13006480 | 1.000 | 0.080 | 2 | 27764354 | intergenic variant | C/G;T | snv | 1 | |||
rs13041834 | 1.000 | 0.080 | 20 | 54086745 | intergenic variant | T/C | snv | 0.42 | 1 | ||
rs6667242 | 1.000 | 0.080 | 1 | 21500073 | intergenic variant | A/G | snv | 0.16 | 1 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 1 | |
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 1 | |
rs7328064 | 1.000 | 0.080 | 13 | 42171982 | intron variant | A/C | snv | 0.11 | 1 | ||
rs6928986 | 1.000 | 0.080 | 6 | 131002852 | intron variant | C/T | snv | 0.78 | 1 | ||
rs7206790 | 0.925 | 0.160 | 16 | 53763996 | intron variant | C/G | snv | 0.49 | 1 | ||
rs6975977 | 1.000 | 0.080 | 7 | 30878216 | intron variant | G/A | snv | 7.3E-02 | 1 | ||
rs35747824 | 1.000 | 0.080 | 16 | 20381986 | intron variant | A/T | snv | 0.24 | 1 | ||
rs74956940 | 1.000 | 0.080 | 19 | 14461154 | intron variant | C/G | snv | 0.15 | 1 | ||
rs121907892 | 0.807 | 0.240 | 11 | 64593747 | stop gained | G/A;C | snv | 2.8E-04 | 1 | ||
rs7076156 | 0.925 | 0.120 | 10 | 62655424 | missense variant | A/C;G | snv | 0.80 | 1 |