Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs605066 | 6 | 139508529 | intron variant | C/T | snv | 0.53 | 6 | ||||
rs645040 | 3 | 136207780 | upstream gene variant | G/T | snv | 0.77 | 6 | ||||
rs718314 | 0.882 | 0.120 | 12 | 26300350 | intron variant | A/G | snv | 0.27 | 6 | ||
rs15285 | 1.000 | 0.040 | 8 | 19967156 | 3 prime UTR variant | C/T | snv | 0.36 | 5 | ||
rs2845885 | 11 | 64101590 | intron variant | C/T | snv | 0.87 | 5 | ||||
rs634869 | 6 | 139510620 | intron variant | T/A;C | snv | 5 | |||||
rs72959041 | 6 | 127133748 | intron variant | G/A | snv | 3.2E-02 | 5 | ||||
rs9991328 | 4 | 88791970 | intron variant | C/T | snv | 0.53 | 5 | ||||
rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 4 | ||||
rs2207132 | 20 | 40513876 | intergenic variant | G/A | snv | 2.7E-02 | 4 | ||||
rs78058190 | 2 | 218835276 | upstream gene variant | G/A | snv | 3.9E-02 | 4 | ||||
rs900399 | 3 | 157080943 | upstream gene variant | A/G | snv | 0.36 | 4 | ||||
rs4660808 | 1 | 39552837 | intron variant | C/T | snv | 0.17 | 3 | ||||
rs4738141 | 8 | 71557507 | intron variant | A/G | snv | 0.41 | 3 | ||||
rs10101067 | 8 | 71495139 | intron variant | G/C | snv | 6.2E-02 | 2 | ||||
rs3851294 | 1 | 205161285 | missense variant | A/G;T | snv | 0.93 | 2 | ||||
rs56271783 | 11 | 64237251 | intron variant | G/A;C;T | snv | 3.6E-05; 3.7E-02 | 2 | ||||
rs797486 | 13 | 50647482 | intron variant | C/A | snv | 0.85 | 2 |