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 | ||
rs10490924 | 0.716 | 0.240 | 10 | 122454932 | missense variant | G/T | snv | 0.26 | 0.23 | 16 | |
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 | |
rs1064039 | 0.827 | 0.200 | 20 | 23637790 | missense variant | C/G;T | snv | 0.20 | 6 | ||
rs1065489 | 0.695 | 0.440 | 1 | 196740644 | missense variant | G/T | snv | 0.20 | 0.15 | 19 | |
rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 9 | ||
rs10781182 | 0.851 | 0.040 | 9 | 74002804 | intergenic variant | T/G | snv | 0.54 | 4 | ||
rs10922109 | 0.827 | 0.080 | 1 | 196735502 | intron variant | C/A | snv | 0.46 | 6 | ||
rs11080055 | 0.851 | 0.040 | 17 | 28322698 | intron variant | A/C | snv | 0.54 | 5 | ||
rs11200638 | 0.724 | 0.280 | 10 | 122461028 | non coding transcript exon variant | G/A | snv | 0.23 | 14 | ||
rs1136287 | 0.790 | 0.280 | 17 | 1769982 | missense variant | C/T | snv | 0.61 | 0.69 | 8 | |
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 | ||
rs121913059 | 0.716 | 0.280 | 1 | 196747245 | missense variant | C/T | snv | 1.4E-04 | 1.9E-04 | 16 | |
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 | |
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 |