Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10036789 | 1.000 | 0.080 | 5 | 72400091 | regulatory region variant | C/A;G | snv | 3 | |||
rs10044254 | 0.925 | 0.080 | 5 | 15783487 | intron variant | A/G | snv | 0.25 | 2 | ||
rs10158467 | 0.925 | 0.080 | 1 | 173162354 | regulatory region variant | A/G;T | snv | 2 | |||
rs10175070 | 1.000 | 0.080 | 2 | 227805859 | 5 prime UTR variant | G/A;C | snv | 1 | |||
rs10187276 | 0.925 | 0.080 | 2 | 227805721 | upstream gene variant | T/C | snv | 0.62 | 2 | ||
rs10208293 | 0.882 | 0.160 | 2 | 102349850 | intron variant | G/A | snv | 0.33 | 4 | ||
rs10414065 | 0.882 | 0.080 | 19 | 33230549 | upstream gene variant | C/T | snv | 5.5E-02 | 4 | ||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs10445308 | 0.851 | 0.240 | 17 | 39781794 | intron variant | C/T | snv | 0.38 | 5 | ||
rs10494132 | 0.851 | 0.080 | 1 | 111289601 | upstream gene variant | T/C | snv | 0.26 | 4 | ||
rs10519031 | 1.000 | 0.080 | 15 | 59890806 | regulatory region variant | T/C | snv | 2.2E-02 | 1 | ||
rs10767664 | 0.752 | 0.400 | 11 | 27704439 | intron variant | T/A | snv | 0.83 | 16 | ||
rs10774625 | 0.763 | 0.320 | 12 | 111472415 | intron variant | A/G | snv | 0.66 | 13 | ||
rs10830123 | 1.000 | 0.080 | 10 | 127551386 | intron variant | G/C | snv | 0.29 | 1 | ||
rs10836538 | 0.925 | 0.080 | 11 | 36343703 | intron variant | G/T | snv | 0.30 | 2 | ||
rs10924993 | 0.925 | 0.080 | 1 | 236296485 | intergenic variant | T/A;G | snv | 2 | |||
rs10995245 | 0.882 | 0.160 | 10 | 62631615 | intron variant | G/A;C | snv | 3 | |||
rs11000019 | 1.000 | 0.080 | 10 | 71831773 | intron variant | G/A | snv | 3.3E-02 | 1 | ||
rs11021111 | 1.000 | 0.080 | 11 | 95270099 | intergenic variant | C/G | snv | 4.3E-02 | 1 | ||
rs1102705 | 0.925 | 0.080 | 1 | 172731728 | intergenic variant | G/A | snv | 0.93 | 3 | ||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs11071559 | 0.925 | 0.080 | 15 | 60777789 | intron variant | C/T | snv | 0.23 | 4 | ||
rs1117490 | 0.925 | 0.080 | 6 | 30202733 | intron variant | T/C | snv | 0.24 | 2 | ||
rs11178648 | 0.925 | 0.080 | 12 | 71139430 | intron variant | C/T | snv | 0.29 | 2 |