Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10001106 | 0.925 | 0.120 | 4 | 10125817 | intergenic variant | T/A;C | snv | 3 | |||
rs10001632 | 0.925 | 0.120 | 4 | 10520247 | intron variant | A/C | snv | 0.97 | 2 | ||
rs10001964 | 0.925 | 0.120 | 4 | 9957651 | intron variant | C/T | snv | 0.48 | 3 | ||
rs10002984 | 0.925 | 0.120 | 4 | 9679109 | intron variant | T/C | snv | 0.95 | 2 | ||
rs10003001 | 0.925 | 0.120 | 4 | 9982851 | intron variant | C/T | snv | 0.21 | 3 | ||
rs10003864 | 0.925 | 0.120 | 4 | 10435767 | downstream gene variant | T/C | snv | 0.29 | 3 | ||
rs10005684 | 0.925 | 0.120 | 4 | 9625273 | intron variant | T/A;G | snv | 2 | |||
rs10006397 | 0.925 | 0.120 | 4 | 10034516 | non coding transcript exon variant | C/A | snv | 0.78 | 3 | ||
rs1000662 | 0.925 | 0.120 | 11 | 64466347 | intergenic variant | G/A | snv | 0.60 | 2 | ||
rs10007469 | 0.925 | 0.120 | 4 | 9731119 | upstream gene variant | G/A;C;T | snv | 2 | |||
rs10008035 | 0.925 | 0.120 | 4 | 9997711 | intron variant | G/A;T | snv | 3 | |||
rs10009493 | 0.925 | 0.120 | 4 | 10130423 | intergenic variant | C/G | snv | 0.18 | 3 | ||
rs10009618 | 0.925 | 0.120 | 4 | 88172856 | intron variant | C/T | snv | 0.58 | 3 | ||
rs10010656 | 0.925 | 0.120 | 4 | 10244703 | intergenic variant | G/C | snv | 0.30 | 3 | ||
rs10011206 | 0.925 | 0.120 | 4 | 9990331 | intron variant | C/T | snv | 0.23 | 3 | ||
rs10011621 | 0.925 | 0.120 | 4 | 9758615 | downstream gene variant | A/C | snv | 0.22 | 2 | ||
rs10011796 | 0.882 | 0.160 | 4 | 88169725 | intron variant | T/C;G | snv | 4 | |||
rs1001216 | 0.925 | 0.120 | 4 | 10167225 | non coding transcript exon variant | A/G | snv | 0.15 | 3 | ||
rs1001217 | 0.925 | 0.120 | 4 | 10167375 | non coding transcript exon variant | C/A;G | snv | 3 | |||
rs10012288 | 0.925 | 0.120 | 4 | 10139329 | downstream gene variant | G/A | snv | 0.42 | 3 | ||
rs10012779 | 0.925 | 0.120 | 4 | 10036488 | intron variant | C/T | snv | 0.15 | 3 | ||
rs10013288 | 0.925 | 0.120 | 4 | 9557597 | upstream gene variant | T/A;G | snv | 2 | |||
rs10015494 | 0.925 | 0.120 | 4 | 10140366 | downstream gene variant | G/A;C;T | snv | 3 | |||
rs10015872 | 0.925 | 0.120 | 4 | 10140786 | downstream gene variant | G/A | snv | 0.42 | 3 | ||
rs10016022 | 0.925 | 0.120 | 4 | 10445282 | missense variant | A/G;T | snv | 0.74 | 3 |