Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
rs7394579 | 1.000 | 0.080 | 11 | 61813978 | intron variant | A/G | snv | 0.22 | 5 | ||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 4 | ||
rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs74847330 | 2 | 143074030 | intergenic variant | A/G | snv | 8.8E-02 | 4 | ||||
rs7896518 | 10 | 63344740 | intron variant | A/G | snv | 0.38 | 4 | ||||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 4 | |||
rs1059196 | 22 | 19724571 | 3 prime UTR variant | C/T | snv | 0.42 | 3 | ||||
rs10761741 | 1.000 | 0.040 | 10 | 63306426 | intron variant | G/T | snv | 0.38 | 3 | ||
rs10886430 | 10 | 119250744 | intron variant | A/G | snv | 8.8E-02 | 3 | ||||
rs11071720 | 15 | 63049797 | intron variant | T/C;G | snv | 3 | |||||
rs11734132 | 4 | 6889792 | intergenic variant | G/C | snv | 0.17 | 3 | ||||
rs117672662 | 14 | 68958750 | intron variant | T/C | snv | 7.4E-03 | 3 | ||||
rs12041331 | 0.776 | 0.200 | 1 | 156899922 | intron variant | G/A | snv | 0.19 | 3 | ||
rs12445050 | 16 | 81837364 | intron variant | C/T | snv | 9.6E-02 | 3 | ||||
rs139141690 | 7 | 101856650 | intron variant | G/A | snv | 2.2E-03 | 3 | ||||
rs17116384 | 11 | 114110519 | intron variant | A/G | snv | 0.25 | 3 | ||||
rs17396340 | 1 | 10226118 | intron variant | G/A;C | snv | 3 | |||||
rs17572109 | 2 | 218229211 | non coding transcript exon variant | G/A;T | snv | 3 | |||||
rs2157770 | 9 | 134056342 | intron variant | A/G | snv | 0.33 | 3 | ||||
rs2393967 | 10 | 63373396 | intron variant | A/C | snv | 0.23 | 3 | ||||
rs342293 | 0.882 | 0.040 | 7 | 106731773 | intron variant | C/G | snv | 0.42 | 3 | ||
rs35150201 | 7 | 135661514 | upstream gene variant | T/G | snv | 0.42 | 3 | ||||
rs3804749 | 3 | 123114156 | intron variant | C/T | snv | 0.48 | 3 |