Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104893751 | 0.882 | 0.240 | 3 | 9750423 | missense variant | G/A;C | snv | 2.2E-03; 4.0E-06 | 5 | ||
rs104893877 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 59 | |||
rs104894002 | 0.790 | 0.320 | 6 | 41161557 | stop gained | G/A | snv | 2.0E-05 | 2.1E-05 | 7 | |
rs1049296 | 0.882 | 0.120 | 3 | 133775510 | missense variant | C/T | snv | 0.16 | 0.14 | 4 | |
rs1049564 | 0.882 | 0.160 | 14 | 20472447 | missense variant | G/A | snv | 0.19 | 0.21 | 6 | |
rs10498633 | 0.925 | 0.080 | 14 | 92460608 | intron variant | G/T | snv | 0.19 | 2 | ||
rs10501320 | 0.925 | 0.120 | 11 | 47272248 | 5 prime UTR variant | G/C | snv | 0.17 | 5 | ||
rs10501602 | 1.000 | 0.080 | 11 | 85970346 | intron variant | A/G | snv | 0.10 | 1 | ||
rs1050210428 | 0.925 | 0.120 | 17 | 45983258 | missense variant | G/A | snv | 2 | |||
rs1050283 | 0.882 | 0.160 | 12 | 10159690 | 3 prime UTR variant | G/A | snv | 0.40 | 4 | ||
rs1050565 | 1.000 | 0.080 | 17 | 30249058 | missense variant | T/C | snv | 0.30 | 0.29 | 2 | |
rs10507391 | 0.776 | 0.320 | 13 | 30737959 | intron variant | A/T | snv | 0.52 | 10 | ||
rs1051266 | 0.627 | 0.640 | 21 | 45537880 | missense variant | T/C;G | snv | 0.55; 4.4E-06 | 41 | ||
rs1051338 | 0.807 | 0.120 | 10 | 89247603 | missense variant | T/G | snv | 0.32 | 0.26 | 7 | |
rs10515639 | 1.000 | 0.080 | 5 | 150276863 | intron variant | C/T | snv | 0.24 | 1 | ||
rs10516846 | 1.000 | 0.080 | 4 | 89775184 | intron variant | A/G | snv | 3.9E-02 | 1 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs10524523 | 0.807 | 0.200 | 19 | 44899792 | intron variant | TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT | delins | 7 | |||
rs1057233 | 1.000 | 0.080 | 11 | 47354897 | 3 prime UTR variant | G/A | snv | 0.69 | 1 | ||
rs1057518919 | 0.851 | 0.120 | 14 | 73171023 | missense variant | T/G | snv | 5 | |||
rs1057519991 | 0.662 | 0.440 | 17 | 7675076 | missense variant | T/A;C;G | snv | 4.0E-06 | 26 | ||
rs1057520247 | 0.882 | 0.200 | 13 | 32326591 | synonymous variant | C/T | snv | 7.0E-06 | 5 | ||
rs1060620 | 1.000 | 0.080 | 12 | 6535556 | intron variant | A/G;T | snv | 0.32 | 1 | ||
rs1060743 | 0.925 | 0.080 | 2 | 127068957 | synonymous variant | A/G | snv | 0.34 | 0.29 | 2 | |
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 72 |