Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10033900 | 0.807 | 0.040 | 4 | 109737911 | intron variant | T/C | snv | 0.54 | 7 | ||
rs10781182 | 0.851 | 0.040 | 9 | 74002804 | intergenic variant | T/G | snv | 0.54 | 4 | ||
rs11080055 | 0.851 | 0.040 | 17 | 28322698 | intron variant | A/C | snv | 0.54 | 5 | ||
rs114092250 | 0.851 | 0.040 | 5 | 35494346 | intergenic variant | G/A;T | snv | 4 | |||
rs1142 | 0.851 | 0.040 | 7 | 105115879 | intron variant | C/T | snv | 0.31 | 6 | ||
rs114254831 | 0.827 | 0.040 | 6 | 32187804 | intron variant | A/G | snv | 5 | |||
rs116503776 | 0.827 | 0.040 | 6 | 31962685 | intron variant | G/A | snv | 5 | |||
rs11884770 | 0.851 | 0.040 | 2 | 227222204 | intron variant | T/A;C | snv | 4 | |||
rs12019136 | 0.851 | 0.040 | 19 | 5835666 | intron variant | G/A | snv | 0.12 | 4 | ||
rs12357257 | 0.851 | 0.040 | 10 | 24710664 | intron variant | G/A | snv | 0.18 | 4 | ||
rs12661281 | 0.882 | 0.040 | 6 | 31874821 | missense variant | T/A | snv | 0.15 | 0.11 | 3 | |
rs13095226 | 0.851 | 0.040 | 3 | 99677428 | intron variant | T/C | snv | 9.5E-02 | 5 | ||
rs140647181 | 0.851 | 0.040 | 3 | 99461824 | intergenic variant | T/C | snv | 1.5E-02 | 4 | ||
rs141853578 | 0.807 | 0.040 | 4 | 109764664 | missense variant | C/T | snv | 4.2E-04 | 3.9E-04 | 6 | |
rs142450006 | 0.851 | 0.040 | 20 | 45986353 | regulatory region variant | TTCT/-;TTCTTTCT | delins | 2.0E-02 | 4 | ||
rs147859257 | 0.827 | 0.040 | 19 | 6718135 | missense variant | T/G | snv | 2.8E-03 | 2.4E-03 | 6 | |
rs148553336 | 0.851 | 0.040 | 1 | 196644043 | intergenic variant | T/C | snv | 7.7E-03 | 4 | ||
rs17231506 | 0.851 | 0.040 | 16 | 56960616 | upstream gene variant | C/G;T | snv | 0.28 | 10 | ||
rs181705462 | 0.851 | 0.040 | 6 | 31979250 | intron variant | G/C;T | snv | 4 | |||
rs187328863 | 0.851 | 0.040 | 1 | 196411028 | intron variant | C/T | snv | 1.6E-02 | 4 | ||
rs191281603 | 0.851 | 0.040 | 1 | 196989521 | intron variant | C/G;T | snv | 4.6E-03 | 4 | ||
rs1999930 | 0.882 | 0.040 | 6 | 116065971 | intergenic variant | C/A;G;T | snv | 3 | |||
rs201459901 | 0.851 | 0.040 | 20 | 58078668 | regulatory region variant | -/A | delins | 0.21 | 4 | ||
rs2284665 | 0.882 | 0.040 | 10 | 122467114 | intron variant | G/A;T | snv | 3 | |||
rs2285714 | 0.882 | 0.040 | 4 | 109717654 | synonymous variant | C/T | snv | 0.37 | 0.31 | 3 |