Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 8 | ||
rs10484560 | 1.000 | 0.120 | 6 | 32330360 | intron variant | G/A | snv | 8.6E-02 | 1 | ||
rs10484565 | 0.925 | 0.200 | 6 | 32827255 | 3 prime UTR variant | G/A | snv | 6.1E-02 | 2 | ||
rs10484566 | 0.925 | 0.200 | 6 | 32867481 | regulatory region variant | T/G | snv | 6.8E-02 | 2 | ||
rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 7 | ||
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 1 | ||
rs1049281 | 1.000 | 0.120 | 6 | 31268790 | 3 prime UTR variant | T/C | snv | 0.68 | 1 | ||
rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 2 | ||
rs1050152 | 0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 | 1 | |
rs1051336 | 0.925 | 0.120 | 6 | 32444815 | 3 prime UTR variant | G/A;C | snv | 0.15 | 1 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 2 | ||
rs1051794 | 0.925 | 0.120 | 6 | 31411332 | missense variant | G/A | snv | 0.34 | 0.35 | 4 | |
rs1052248 | 1.000 | 0.120 | 6 | 31588804 | 3 prime UTR variant | T/A | snv | 0.26 | 1 | ||
rs1055569 | 0.882 | 0.240 | 6 | 31472305 | non coding transcript exon variant | C/T | snv | 0.41 | 2 | ||
rs1059288 | 0.882 | 0.320 | 6 | 33299895 | 3 prime UTR variant | A/G | snv | 0.60 | 1 | ||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 1 | |
rs1063355 | 0.827 | 0.320 | 6 | 32659937 | 3 prime UTR variant | T/G | snv | 0.56 | 2 | ||
rs1063635 | 1.000 | 0.120 | 6 | 31412154 | missense variant | G/A | snv | 0.50 | 0.54 | 1 | |
rs1075496 | 0.882 | 0.160 | 6 | 30690462 | intron variant | C/A | snv | 0.47 | 1 | ||
rs1076828 | 1.000 | 0.120 | 6 | 30660475 | non coding transcript exon variant | G/A | snv | 0.29 | 1 | ||
rs1076832 | 1.000 | 0.120 | 6 | 30452054 | non coding transcript exon variant | C/A | snv | 0.15 | 1 | ||
rs1077393 | 0.882 | 0.200 | 6 | 31642752 | non coding transcript exon variant | A/G | snv | 0.44 | 3 | ||
rs10774624 | 0.882 | 0.160 | 12 | 111395984 | intron variant | G/A | snv | 0.67 | 1 | ||
rs10790268 | 1.000 | 0.120 | 11 | 118858682 | intergenic variant | A/G;T | snv | 1 | |||
rs10795791 | 0.925 | 0.200 | 10 | 6066377 | upstream gene variant | A/G | snv | 0.40 | 1 |