Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 25 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 17 | |||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs8050136 | 0.716 | 0.560 | 16 | 53782363 | intron variant | C/A | snv | 0.40 | 9 | ||
rs2074356 | 0.763 | 0.280 | 12 | 112207597 | intron variant | G/A | snv | 3.8E-03 | 9 | ||
rs963837 | 0.925 | 0.120 | 11 | 30727543 | intergenic variant | T/C | snv | 0.35 | 8 | ||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 8 | ||
rs11642015 | 0.925 | 0.120 | 16 | 53768582 | intron variant | C/T | snv | 0.31 | 7 | ||
rs760077 | 0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 | 7 | ||
rs77924615 | 1.000 | 0.080 | 16 | 20381010 | intron variant | G/A | snv | 0.16 | 7 | ||
rs1533988 | 7 | 1253374 | intergenic variant | A/T | snv | 0.59 | 6 | ||||
rs17216707 | 20 | 54115823 | intergenic variant | T/C | snv | 0.17 | 6 | ||||
rs3925584 | 1.000 | 0.080 | 11 | 30738788 | intergenic variant | T/C | snv | 0.35 | 6 | ||
rs17050272 | 0.882 | 0.120 | 2 | 120548864 | upstream gene variant | G/A | snv | 0.33 | 6 | ||
rs4976646 | 0.851 | 0.200 | 5 | 177361569 | intron variant | T/C | snv | 0.41 | 6 | ||
rs2823139 | 1.000 | 0.080 | 21 | 15204463 | intron variant | G/A | snv | 0.34 | 5 | ||
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 5 | ||
rs8096658 | 0.925 | 0.120 | 18 | 79396537 | intron variant | C/G | snv | 0.39 | 5 | ||
rs7123489 | 1.000 | 0.080 | 11 | 65756781 | intron variant | C/A | snv | 0.29 | 4 | ||
rs8176644 | 9 | 133273734 | intron variant | C/T | snv | 4 | |||||
rs2470893 | 0.882 | 0.160 | 15 | 74727108 | upstream gene variant | C/T | snv | 0.20 | 4 | ||
rs6026578 | 20 | 58888417 | 5 prime UTR variant | C/G | snv | 0.60 | 4 | ||||
rs80282103 | 1.000 | 0.080 | 10 | 853131 | intron variant | A/T | snv | 0.12 | 4 |