| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10041756 | 1.000 | 0.040 | 5 | 22996131 | intergenic variant | G/A | snv | 0.14 | 1 | ||
| rs10043333 | 1.000 | 0.040 | 5 | 158816761 | intron variant | C/G;T | snv | 1 | |||
| rs10043478 | 1.000 | 0.040 | 5 | 138853022 | intron variant | G/C | snv | 0.67 | 1 | ||
| rs10046678 | 1.000 | 0.040 | 8 | 23958610 | intergenic variant | T/G | snv | 0.20 | 1 | ||
| rs10048683 | 1.000 | 0.040 | 2 | 26097650 | intron variant | G/A | snv | 0.77 | 1 | ||
| rs10050141 | 1.000 | 0.040 | 4 | 76530384 | intron variant | G/A | snv | 9.0E-02 | 1 | ||
| rs10052628 | 1.000 | 0.040 | 5 | 25949752 | intergenic variant | C/T | snv | 7.8E-02 | 1 | ||
| rs10053503 | 1.000 | 0.040 | 5 | 104778862 | intron variant | T/G | snv | 8.3E-02 | 1 | ||
| rs10053765 | 1.000 | 0.040 | 5 | 99658228 | intergenic variant | T/C | snv | 0.49 | 1 | ||
| rs10054105 | 0.925 | 0.080 | 5 | 111573636 | intron variant | T/G | snv | 0.17 | 3 | ||
| rs10054454 | 1.000 | 0.040 | 5 | 78264811 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs10057744 | 1.000 | 0.040 | 5 | 170109750 | downstream gene variant | C/T | snv | 0.89 | 1 | ||
| rs1006066 | 1.000 | 0.040 | 6 | 17679884 | intron variant | G/C | snv | 0.11 | 1 | ||
| rs10061629 | 1.000 | 0.040 | 5 | 77369396 | intron variant | C/G;T | snv | 1 | |||
| rs10061900 | 1.000 | 0.040 | 5 | 158826534 | intron variant | T/C | snv | 0.59 | 1 | ||
| rs10062083 | 1.000 | 0.040 | 5 | 9130861 | intron variant | A/C | snv | 0.11 | 1 | ||
| rs10062992 | 1.000 | 0.040 | 5 | 98143166 | intron variant | G/A | snv | 0.52 | 1 | ||
| rs10063003 | 1.000 | 0.040 | 5 | 98143216 | intron variant | G/A | snv | 0.54 | 1 | ||
| rs10063061 | 1.000 | 0.040 | 5 | 126608051 | intron variant | A/C | snv | 0.26 | 1 | ||
| rs10063424 | 1.000 | 0.040 | 5 | 170108518 | synonymous variant | T/C | snv | 0.91 | 0.90 | 1 | |
| rs10064820 | 1.000 | 0.040 | 5 | 39324690 | intron variant | G/A | snv | 3.1E-02 | 1 | ||
| rs10064843 | 1.000 | 0.040 | 5 | 25948342 | regulatory region variant | G/A | snv | 0.17 | 1 | ||
| rs10067455 | 1.000 | 0.040 | 5 | 88162105 | intergenic variant | G/T | snv | 0.82 | 1 | ||
| rs10067626 | 1.000 | 0.040 | 5 | 31914860 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs10069142 | 1.000 | 0.040 | 5 | 115777468 | upstream gene variant | A/G;T | snv | 1 |