Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10033464 | 0.807 | 0.200 | 4 | 110799605 | downstream gene variant | T/G | snv | 0.86 | 1 | ||
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 5 | |
rs10093110 | 1.000 | 0.040 | 8 | 105553186 | intron variant | G/A;T | snv | 1 | |||
rs10106652 | 1.000 | 0.040 | 8 | 20070649 | intergenic variant | G/A | snv | 0.29 | 3 | ||
rs10128951 | 1.000 | 0.040 | 12 | 124855901 | intron variant | G/A | snv | 0.47 | 1 | ||
rs10131519 | 1.000 | 0.040 | 14 | 99892957 | intron variant | T/C | snv | 0.29 | 1 | ||
rs10131894 | 1.000 | 0.040 | 14 | 74980176 | regulatory region variant | C/G | snv | 0.49 | 2 | ||
rs10139550 | 1.000 | 0.040 | 14 | 99679373 | 3 prime UTR variant | C/G | snv | 0.39 | 1 | ||
rs10186133 | 1.000 | 0.040 | 2 | 113079367 | downstream gene variant | G/A;T | snv | 1 | |||
rs10221742 | 1.000 | 0.040 | 2 | 21196778 | downstream gene variant | G/A | snv | 0.32 | 1 | ||
rs10237377 | 1.000 | 0.040 | 7 | 140057336 | intron variant | G/T | snv | 0.48 | 1 | ||
rs10249651 | 1.000 | 0.040 | 7 | 117424571 | intron variant | T/C | snv | 0.40 | 1 | ||
rs10267593 | 1.000 | 0.040 | 7 | 1897625 | intron variant | G/A | snv | 0.25 | 1 | ||
rs1034246 | 1.000 | 0.040 | 6 | 43100632 | intron variant | G/T | snv | 0.19 | 1 | ||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 22 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 10 | ||
rs10456100 | 1.000 | 0.040 | 6 | 39215694 | intron variant | C/T | snv | 0.20 | 2 | ||
rs1048990 | 0.790 | 0.280 | 14 | 35292469 | 5 prime UTR variant | C/G;T | snv | 0.19; 4.0E-06 | 1 | ||
rs10495907 | 1.000 | 0.040 | 2 | 43771587 | upstream gene variant | G/A | snv | 0.13 | 1 | ||
rs1050362 | 1.000 | 0.040 | 16 | 72096916 | missense variant | C/A;T | snv | 0.38; 2.4E-05 | 1 | ||
rs10512861 | 1.000 | 0.040 | 3 | 132539117 | downstream gene variant | G/A;T | snv | 1 | |||
rs1051338 | 0.807 | 0.120 | 10 | 89247603 | missense variant | T/G | snv | 0.32 | 0.26 | 1 | |
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 5 | |
rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 2 | ||
rs1065852 | 0.695 | 0.360 | 22 | 42130692 | missense variant | G/A | snv | 0.21 | 0.19 | 2 |