| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs111970895 | 1.000 | 0.120 | 5 | 102301953 | upstream gene variant | -/AAA;AAAAAA | delins | 1 | |||
| rs12025262 | 1.000 | 0.120 | 1 | 247193430 | intron variant | G/A;C;T | snv | 1 | |||
| rs12031579 | 1.000 | 0.120 | 1 | 119307920 | intron variant | G/A | snv | 6.8E-02 | 1 | ||
| rs137672 | 1.000 | 0.120 | 22 | 39341089 | intergenic variant | C/T | snv | 0.40 | 1 | ||
| rs144199732 | 1.000 | 0.120 | X | 43022624 | intergenic variant | C/T | snv | 1.2E-02 | 1 | ||
| rs145065165 | 1.000 | 0.120 | 16 | 55347327 | intergenic variant | G/A | snv | 1.0E-03 | 1 | ||
| rs169225 | 1.000 | 0.120 | 20 | 22393040 | intron variant | T/G | snv | 0.42 | 1 | ||
| rs295315 | 1.000 | 0.120 | 3 | 141643383 | intergenic variant | A/C;G | snv | 1 | |||
| rs34097398 | 1.000 | 0.120 | X | 33452415 | intergenic variant | A/-;AA;AAA;AAAA;AAAAA | delins | 1 | |||
| rs34344307 | 1.000 | 0.120 | 16 | 77008512 | intergenic variant | TTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT | delins | 1 | |||
| rs561504284 | 1.000 | 0.120 | 17 | 46262887 | upstream gene variant | A/G | snv | 1 | |||
| rs6134303 | 1.000 | 0.120 | 20 | 11586401 | intergenic variant | T/G | snv | 0.67 | 1 | ||
| rs66696671 | 1.000 | 0.120 | 10 | 119607441 | intergenic variant | G/T | snv | 0.25 | 1 | ||
| rs75921351 | 1.000 | 0.120 | 16 | 54596587 | intergenic variant | C/T | snv | 3.1E-03 | 1 | ||
| rs8069681 | 1.000 | 0.120 | 17 | 5064847 | downstream gene variant | A/G;T | snv | 1 | |||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs2229109 | 0.807 | 0.240 | 7 | 87550493 | missense variant | C/A;T | snv | 2.7E-02 | 8 | ||
| rs35068177 | 0.882 | 0.120 | 7 | 87550213 | synonymous variant | T/C | snv | 2.2E-04 | 3.1E-04 | 3 | |
| rs1327418487 | 1.000 | 0.120 | 4 | 83462555 | frameshift variant | -/T | delins | 7.0E-05 | 1 | ||
| rs12658731 | 1.000 | 0.120 | 5 | 5169477 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs145022376 | 1.000 | 0.120 | 10 | 1186289 | intron variant | C/- | delins | 9.1E-03 | 1 | ||
| rs186724 | 0.882 | 0.120 | 1 | 110018293 | intron variant | C/G;T | snv | 3 | |||
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs2363956 | 0.776 | 0.160 | 19 | 17283315 | missense variant | T/G | snv | 0.48 | 0.50 | 8 | |
| rs1801155 | 0.649 | 0.440 | 5 | 112839514 | missense variant | T/A | snv | 8.0E-06; 2.0E-03 | 1.2E-03 | 42 |