Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 9 | ||
rs62435145 | 1.000 | 0.040 | 7 | 1246931 | regulatory region variant | G/T | snv | 0.51 | 8 | ||
rs3765209 | 0.851 | 0.040 | 21 | 15417030 | intron variant | C/T | snv | 0.31 | 7 | ||
rs4810479 | 1.000 | 0.040 | 20 | 45916409 | upstream gene variant | C/T | snv | 0.68 | 7 | ||
rs13146355 | 1.000 | 0.040 | 4 | 76490987 | intron variant | G/A | snv | 0.33 | 6 | ||
rs11920090 | 1.000 | 0.040 | 3 | 170999732 | intron variant | T/A | snv | 0.20 | 5 | ||
rs12922822 | 1.000 | 0.040 | 16 | 20356323 | upstream gene variant | C/A;T | snv | 5 | |||
rs3789678 | 1.000 | 0.040 | 1 | 230713736 | intron variant | C/T | snv | 0.15 | 5 | ||
rs7936247 | 1.000 | 0.040 | 11 | 92956866 | intergenic variant | G/T | snv | 0.37 | 5 | ||
rs1264347 | 1.000 | 0.040 | 6 | 30830920 | upstream gene variant | C/T | snv | 7.9E-02 | 4 | ||
rs36217263 | 1.000 | 0.040 | 13 | 33015697 | upstream gene variant | A/- | del | 0.21 | 4 | ||
rs3812035 | 1.000 | 0.040 | 5 | 177390142 | 3 prime UTR variant | G/A;T | snv | 4 | |||
rs10084572 | 1.000 | 0.040 | 21 | 43992991 | downstream gene variant | T/A;C;G | snv | 3 | |||
rs1052700 | 1.000 | 0.040 | 15 | 89665079 | 3 prime UTR variant | A/T | snv | 0.26 | 3 | ||
rs10941191 | 1.000 | 0.040 | 5 | 34504693 | intergenic variant | C/A;T | snv | 3 | |||
rs11071657 | 1.000 | 0.040 | 15 | 62141763 | regulatory region variant | A/G | snv | 0.31 | 3 | ||
rs11124945 | 1.000 | 0.040 | 2 | 43650017 | intron variant | A/G | snv | 0.21 | 3 | ||
rs113296370 | 1.000 | 0.040 | 2 | 43636315 | upstream gene variant | A/C | snv | 0.17 | 3 | ||
rs12107 | 1.000 | 0.040 | 22 | 36281936 | 3 prime UTR variant | G/A;T | snv | 3 | |||
rs1228534100 | 1.000 | 0.040 | 12 | 120978892 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
rs145590578 | 1.000 | 0.040 | 6 | 160236104 | intron variant | GTT/- | delins | 9.8E-02 | 3 | ||
rs1556751 | 1.000 | 0.040 | 9 | 68818296 | intron variant | G/A | snv | 0.63 | 3 | ||
rs1906436 | 1.000 | 0.040 | 15 | 53590245 | intron variant | T/C | snv | 0.32 | 3 | ||
rs192902098 | 1.000 | 0.040 | 13 | 27920235 | missense variant | C/A;G;T | snv | 2.6E-03; 3.4E-04; 5.6E-05 | 3 | ||
rs1974990 | 1.000 | 0.040 | 2 | 169790406 | non coding transcript exon variant | G/T | snv | 0.90 | 3 |