Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10085588 | 1.000 | 0.080 | 7 | 96508362 | intron variant | A/G | snv | 0.72 | 3 | ||
rs1107748 | 1.000 | 0.080 | 17 | 43696446 | intron variant | T/C | snv | 0.54 | 3 | ||
rs11898505 | 2 | 54457420 | intron variant | A/G | snv | 0.76 | 2 | ||||
rs1213308971 | X | 31348599 | missense variant | T/A | snv | 5.5E-06 | 1 | ||||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12475342 | 2 | 54655541 | intron variant | G/A | snv | 0.28 | 1 | ||||
rs13182402 | 0.925 | 0.160 | 5 | 126582456 | intron variant | A/G | snv | 0.15 | 4 | ||
rs1427938321 | X | 32365095 | missense variant | T/A | snv | 5.5E-06 | 1 | ||||
rs1643821 | 6 | 151862416 | intron variant | G/A | snv | 0.46 | 2 | ||||
rs17790156 | 11 | 46883767 | intron variant | A/T | snv | 8.9E-02 | 1 | ||||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs1800012 | 0.763 | 0.320 | 17 | 50200388 | intron variant | C/A | snv | 0.14 | 13 | ||
rs1800544 | 0.790 | 0.160 | 10 | 111076745 | upstream gene variant | G/C | snv | 0.59 | 12 | ||
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs1982073 | 0.649 | 0.640 | 19 | 41353016 | missense variant | G/A;C | snv | 32 | |||
rs2073618 | 0.716 | 0.480 | 8 | 118951813 | missense variant | G/C | snv | 0.52 | 0.60 | 19 | |
rs2234693 | 0.555 | 0.680 | 6 | 151842200 | intron variant | T/C | snv | 0.47 | 77 | ||
rs270611 | 5 | 132256377 | intron variant | C/A;T | snv | 1 | |||||
rs281865264 | 1.000 | 0.080 | 11 | 61959539 | missense variant | T/A;C | snv | 4.0E-06 | 2 | ||
rs2908004 | 1.000 | 0.040 | 7 | 121329715 | missense variant | G/A;T | snv | 0.44; 4.0E-06 | 4 | ||
rs2941584 | 2 | 54654484 | intron variant | T/C | snv | 0.64 | 1 | ||||
rs3087456 | 0.742 | 0.480 | 16 | 10877045 | intron variant | G/A | snv | 0.53 | 14 | ||
rs3102734 | 0.925 | 0.080 | 8 | 118951777 | intron variant | G/A | snv | 7.3E-02 | 9.5E-02 | 3 | |
rs3102735 | 0.752 | 0.400 | 8 | 118952831 | upstream gene variant | T/C | snv | 0.17 | 12 | ||
rs3134069 | 0.776 | 0.320 | 8 | 118952749 | upstream gene variant | A/C | snv | 9.6E-02 | 11 |