Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs12579302 | 0.851 | 0.120 | 12 | 89656726 | intron variant | A/G | snv | 0.15 | 19 | ||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 18 | |
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 17 | |
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 14 | ||||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 13 | ||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 12 | ||
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 9 | ||
rs4665972 | 2 | 27375230 | intron variant | T/C | snv | 0.69 | 8 | ||||
rs740746 | 10 | 114033028 | intergenic variant | G/A | snv | 0.70 | 8 | ||||
rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 6 | ||
rs2244608 | 0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 | 6 | ||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 6 | ||||
rs2642438 | 1 | 220796686 | missense variant | A/G | snv | 0.75 | 0.78 | 6 | |||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 6 | |||
rs7096937 | 10 | 112190660 | intron variant | T/C | snv | 0.72 | 5 | ||||
rs9989419 | 0.882 | 0.120 | 16 | 56951227 | regulatory region variant | A/G | snv | 0.55 | 5 | ||
rs13135092 | 4 | 102276925 | intron variant | A/G | snv | 5.1E-02 | 4 | ||||
rs1495743 | 8 | 18415790 | intergenic variant | G/A;C | snv | 4 | |||||
rs1531517 | 1.000 | 0.080 | 19 | 44738916 | intergenic variant | G/A | snv | 0.11 | 4 | ||
rs2043082 | 15 | 58382109 | intron variant | G/A | snv | 0.32 | 4 | ||||
rs2156552 | 1.000 | 0.040 | 18 | 49655298 | downstream gene variant | A/G;T | snv | 4 | |||
rs41274050 | 10 | 50814012 | missense variant | C/A;T | snv | 4.0E-06; 5.3E-03 | 4 | ||||
rs4722551 | 7 | 25952206 | upstream gene variant | T/C;G | snv | 4 |