Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
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 | ||
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 | ||
rs181914721 | 1.000 | 0.040 | 15 | 83819856 | missense variant | G/A | snv | 3.7E-04 | 1.2E-04 | 2 | |
rs17791685 | 1.000 | 0.040 | 3 | 57272583 | 3 prime UTR variant | C/A | snv | 0.19 | 2 | ||
rs15673 | 1.000 | 0.040 | 17 | 68267123 | 3 prime UTR variant | C/A;T | snv | 7.0E-06 | 2 | ||
rs528035 | 1.000 | 0.040 | 3 | 57289142 | intron variant | A/G | snv | 0.48 | 0.37 | 2 | |
rs1042488900 | 1.000 | 0.040 | 1 | 161802188 | synonymous variant | C/T | snv | 2 | |||
rs1060366 | 1.000 | 0.040 | 1 | 116384040 | synonymous variant | A/G | snv | 1.3E-03 | 1.4E-03 | 2 | |
rs575152 | 1.000 | 0.040 | 18 | 79124480 | intron variant | C/T | snv | 0.14 | 2 | ||
rs1042615 | 1.000 | 0.040 | 12 | 63150429 | missense variant | A/C;G;T | snv | 0.60; 1.2E-05 | 2 | ||
rs10747983 | 1.000 | 0.040 | 12 | 63144678 | 3 prime UTR variant | G/A | snv | 0.29 | 2 | ||
rs56381858 | 1.000 | 0.040 | 7 | 80671994 | stop gained | T/C;G | snv | 4.0E-06; 2.4E-04 | 2 | ||
rs768883824 | 1.000 | 0.040 | 7 | 80666481 | missense variant | A/G | snv | 4.0E-06 | 2 |