Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs2243250 | 0.570 | 0.760 | 5 | 132673462 | upstream gene variant | C/T | snv | 0.35 | 61 | ||
rs187084 | 0.641 | 0.480 | 3 | 52227015 | intron variant | A/G | snv | 0.38 | 36 | ||
rs11096957 | 0.790 | 0.160 | 4 | 38774870 | missense variant | T/G | snv | 0.42 | 0.41 | 8 | |
rs12885713 | 0.827 | 0.200 | 14 | 90397013 | intron variant | C/A;G;T | snv | 5 | |||
rs781754383 | 0.882 | 0.080 | 4 | 109960942 | missense variant | C/A;T | snv | 8.0E-06; 4.0E-06 | 3 | ||
rs2243274 | 0.882 | 0.080 | 5 | 132679140 | intron variant | G/A | snv | 0.34 | 3 | ||
rs77245812 | 0.882 | 0.040 | 2 | 20003169 | missense variant | G/A | snv | 1.5E-02 | 1.2E-02 | 3 | |
rs179945 | 0.925 | 0.120 | 6 | 16396238 | intron variant | C/T | snv | 2 | |||
rs752149020 | 0.925 | 0.040 | 2 | 47176459 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs1805013 | 0.925 | 0.120 | 16 | 27362659 | missense variant | C/T | snv | 3.6E-02 | 3.6E-02 | 2 | |
rs1508632 | 1.000 | 0.040 | 6 | 54419678 | intergenic variant | A/G | snv | 0.14 | 1 | ||
rs788748 | 1.000 | 0.040 | 7 | 45986582 | upstream gene variant | A/G | snv | 0.59 | 1 | ||
rs2273650 | 1.000 | 0.040 | 14 | 35401592 | 3 prime UTR variant | C/T | snv | 1.3E-02 | 1 | ||
rs2242190 | 1.000 | 0.040 | 5 | 60548019 | non coding transcript exon variant | C/G | snv | 1 | |||
rs8176070 | 1.000 | 0.040 | 5 | 60541649 | intron variant | G/A;C;T | snv | 0.26 | 1 | ||
rs716508 | 1.000 | 0.040 | 16 | 6286911 | intron variant | C/T | snv | 0.56 | 1 |