Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2073932 | 9 | 133440318 | intron variant | A/G | snv | 0.57 | 1 | ||||
rs652600 | 9 | 133445896 | intron variant | G/A | snv | 0.66 | 1 | ||||
rs536297956 | 13 | 25530064 | missense variant | C/T | snv | 1 | |||||
rs35810727 | 1 | 206112629 | intron variant | G/A;T | snv | 1 | |||||
rs33929415 | 11 | 5225612 | missense variant | G/A;C;T | snv | 4.0E-06 | 1 | ||||
rs587783675 | 11 | 17387104 | missense variant | A/G | snv | 1 | |||||
rs750521766 | 1 | 201389275 | missense variant | C/T | snv | 1.1E-04 | 3.5E-05 | 1 | |||
rs138850469 | 2 | 181678775 | missense variant | G/C | snv | 5.2E-05 | 4.2E-05 | 1 | |||
rs7375036 | 3 | 38727881 | intron variant | T/C | snv | 6.4E-03 | 1 | ||||
rs7712562 | 5 | 1295957 | upstream gene variant | A/G | snv | 0.88 | 1 | ||||
rs10818684 | 1.000 | 0.040 | 9 | 122407651 | intron variant | C/T | snv | 0.62 | 2 | ||
rs1206634 | 1.000 | 0.040 | X | 96302380 | intron variant | T/A;G | snv | 2 | |||
rs1260236 | 1.000 | 0.040 | 9 | 6023030 | intergenic variant | A/G | snv | 2 | |||
rs12910524 | 1.000 | 0.040 | 15 | 101262360 | intergenic variant | T/A;C | snv | 2 | |||
rs1543654 | 1.000 | 0.040 | 21 | 34426752 | upstream gene variant | T/C | snv | 2 | |||
rs181914932 | 1.000 | 0.040 | 20 | 45932640 | non coding transcript exon variant | T/C | snv | 1.6E-02 | 2 | ||
rs2863389 | 1.000 | 0.040 | 3 | 166431104 | intergenic variant | C/T | snv | 0.17 | 2 | ||
rs4258701 | 1.000 | 0.040 | 18 | 27895834 | intergenic variant | C/T | snv | 0.28 | 2 | ||
rs57922 | 1.000 | 0.040 | 5 | 74282114 | intron variant | C/T | snv | 0.40 | 2 | ||
rs649529 | 1.000 | 0.040 | 11 | 88275083 | intergenic variant | G/A;T | snv | 2 | |||
rs6688849 | 1.000 | 0.040 | 1 | 47530532 | intergenic variant | A/C;G | snv | 2 | |||
rs6706313 | 1.000 | 0.040 | 2 | 60311754 | regulatory region variant | A/G | snv | 0.18 | 2 | ||
rs9846911 | 3 | 187500548 | intergenic variant | A/G | snv | 0.47 | 2 | ||||
rs148529020 | 1.000 | 0.040 | 11 | 17460613 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 2 | |
rs756823374 | 1.000 | 0.040 | 11 | 17463515 | missense variant | G/A | snv | 1.4E-05 | 2 |