Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1003878 | 0.882 | 0.200 | 6 | 32332045 | stop gained | G/A | snv | 0.19 | 0.23 | 3 | |
rs1003879 | 1.000 | 0.120 | 6 | 32331815 | intron variant | G/A | snv | 0.41 | 1 | ||
rs1004819 | 0.776 | 0.360 | 1 | 67204530 | intron variant | G/A | snv | 0.30 | 1 | ||
rs10168266 | 0.776 | 0.400 | 2 | 191071078 | intron variant | C/T | snv | 0.19 | 3 | ||
rs10174238 | 0.724 | 0.200 | 2 | 191108308 | intron variant | G/A | snv | 0.70 | 1 | ||
rs10175798 | 1.000 | 0.120 | 2 | 30226728 | upstream gene variant | G/A | snv | 0.51 | 1 | ||
rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 1 | ||
rs1018430 | 1.000 | 0.120 | 6 | 32313911 | intron variant | C/T | snv | 0.25 | 1 | ||
rs1018431 | 1.000 | 0.120 | 6 | 32313899 | intron variant | G/A | snv | 0.25 | 1 | ||
rs1018433 | 1.000 | 0.120 | 6 | 32313733 | intron variant | A/T | snv | 0.21 | 1 | ||
rs1018434 | 1.000 | 0.120 | 6 | 32313583 | intron variant | T/C | snv | 0.21 | 1 | ||
rs10209110 | 1.000 | 0.120 | 2 | 100056230 | intron variant | C/T | snv | 0.47 | 1 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs1033500 | 1.000 | 0.120 | 6 | 32339605 | missense variant | G/A | snv | 0.40 | 0.33 | 2 | |
rs1034323 | 1.000 | 0.120 | 6 | 30400858 | intergenic variant | C/T | snv | 0.43 | 1 | ||
rs1035142 | 0.807 | 0.200 | 2 | 201288355 | 3 prime UTR variant | T/C;G | snv | 0.54 | 1 | ||
rs1041885 | 1.000 | 0.120 | 6 | 32445032 | 3 prime UTR variant | T/A | snv | 0.15 | 1 | ||
rs1042127 | 0.925 | 0.120 | 6 | 31116393 | missense variant | A/C | snv | 0.21 | 0.17 | 1 | |
rs1042337 | 1.000 | 0.120 | 6 | 32937204 | missense variant | G/A | snv | 0.78 | 0.80 | 1 | |
rs1042448 | 1.000 | 0.120 | 6 | 33086565 | 3 prime UTR variant | T/A;C | snv | 6.1E-03; 7.4E-06 | 1 | ||
rs1042544 | 0.925 | 0.200 | 6 | 33086680 | 3 prime UTR variant | A/G | snv | 0.38 | 2 | ||
rs1042663 | 0.925 | 0.160 | 6 | 31937353 | synonymous variant | G/A | snv | 9.7E-02 | 0.12 | 2 | |
rs1043099 | 1.000 | 0.120 | 22 | 30285268 | 3 prime UTR variant | C/A;G;T | snv | 1 | |||
rs1046080 | 1.000 | 0.120 | 6 | 31628105 | missense variant | C/A | snv | 0.79 | 0.74 | 1 | |
rs10484544 | 1.000 | 0.120 | 6 | 29027942 | upstream gene variant | T/C | snv | 0.22 | 1 |