Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10008032 | 1.000 | 0.080 | 4 | 38743861 | intergenic variant | T/C | snv | 0.66 | 2 | ||
rs10021288 | 1.000 | 0.080 | 4 | 122084379 | downstream gene variant | G/A | snv | 0.21 | 1 | ||
rs10036748 | 0.752 | 0.360 | 5 | 151078585 | intron variant | C/A;T | snv | 11 | |||
rs10044254 | 0.925 | 0.080 | 5 | 15783487 | intron variant | A/G | snv | 0.25 | 2 | ||
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 4 | ||
rs10048897 | 1.000 | 0.080 | 22 | 17777938 | non coding transcript exon variant | T/C | snv | 9.9E-02 | 1 | ||
rs10056243 | 1.000 | 0.080 | 5 | 110923378 | intergenic variant | G/A | snv | 8.0E-02 | 1 | ||
rs10056340 | 0.925 | 0.080 | 5 | 110854353 | intergenic variant | T/G | snv | 0.31 | 3 | ||
rs10074523 | 1.000 | 0.080 | 5 | 132724891 | intron variant | C/A | snv | 0.62 | 2 | ||
rs1007654 | 1.000 | 0.080 | 17 | 39955101 | intron variant | A/G | snv | 0.69 | 1 | ||
rs1008723 | 0.925 | 0.160 | 17 | 39910014 | intron variant | G/C;T | snv | 3 | |||
rs1012307 | 1.000 | 0.080 | 2 | 149798707 | intron variant | A/C | snv | 4.9E-02 | 1 | ||
rs10131490 | 1.000 | 0.080 | 14 | 68276590 | intron variant | A/G;T | snv | 1 | |||
rs10142119 | 1.000 | 0.080 | 14 | 98020208 | intergenic variant | G/A;C | snv | 1 | |||
rs10152595 | 1.000 | 0.080 | 15 | 67183150 | intron variant | C/G;T | snv | 2 | |||
rs10158467 | 0.925 | 0.080 | 1 | 173162354 | regulatory region variant | A/G;T | snv | 2 | |||
rs10173081 | 1.000 | 0.080 | 2 | 102340888 | intron variant | C/T | snv | 0.18 | 2 | ||
rs1017494 | 1.000 | 0.080 | 2 | 234770601 | regulatory region variant | C/A;G;T | snv | 2 | |||
rs10174949 | 1.000 | 0.080 | 2 | 8302118 | non coding transcript exon variant | G/A | snv | 0.23 | 2 | ||
rs10178845 | 1.000 | 0.080 | 2 | 8303673 | intron variant | G/A | snv | 0.23 | 2 | ||
rs10187276 | 0.925 | 0.080 | 2 | 227805721 | upstream gene variant | T/C | snv | 0.62 | 2 | ||
rs10189629 | 1.000 | 0.080 | 2 | 102263004 | regulatory region variant | C/A | snv | 0.15 | 2 | ||
rs10192157 | 1.000 | 0.080 | 2 | 102351896 | missense variant | C/T | snv | 0.34 | 0.46 | 2 | |
rs10197862 | 0.925 | 0.120 | 2 | 102350089 | intron variant | A/G | snv | 0.18 | 3 | ||
rs10204137 | 0.925 | 0.160 | 2 | 102351752 | missense variant | A/G;T | snv | 0.34 | 2 |