| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12712127 | 2 | 102110201 | intron variant | A/G | snv | 0.62 | 3 | ||||
| rs1558643 | 2 | 102115231 | intron variant | T/C;G | snv | 1 | |||||
| rs11102001 | 0.925 | 0.080 | 1 | 109757069 | missense variant | G/A | snv | 9.4E-02 | 0.16 | 4 | |
| rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
| rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
| rs4766897 | 12 | 111741667 | intron variant | T/A;C | snv | 1 | |||||
| rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 8 | ||
| rs2420915 | 10 | 121080764 | regulatory region variant | G/A | snv | 0.25 | 1 | ||||
| rs2801231 | 1.000 | 0.080 | X | 122083259 | intergenic variant | T/A;C;G | snv | 2 | |||
| rs1976714 | 3 | 123145924 | intron variant | G/T | snv | 0.32 | 1 | ||||
| rs16834024 | 3 | 123153306 | intron variant | G/A | snv | 5.2E-02 | 1 | ||||
| rs270607 | 5 | 132313493 | intron variant | A/G | snv | 0.69 | 3 | ||||
| rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 6 | |||
| rs10479002 | 5 | 132335969 | synonymous variant | C/G | snv | 1 | |||||
| rs2073643 | 1.000 | 0.080 | 5 | 132387596 | intron variant | T/C | snv | 0.46 | 4 | ||
| rs1016988 | 5 | 132408882 | upstream gene variant | T/C | snv | 0.20 | 4 | ||||
| rs11242111 | 5 | 132420366 | intron variant | A/G;T | snv | 3 | |||||
| rs2106854 | 5 | 132433482 | intron variant | C/T | snv | 0.23 | 3 | ||||
| rs6874639 | 5 | 132443024 | intron variant | A/G | snv | 0.24 | 3 | ||||
| rs1012793 | 5 | 132445653 | intron variant | G/A;C | snv | 1 | |||||
| rs2522056 | 5 | 132466034 | intron variant | G/A | snv | 0.25 | 4 | ||||
| rs2057655 | 5 | 132471932 | non coding transcript exon variant | G/A | snv | 0.24 | 1 | ||||
| rs6873426 | 5 | 132482939 | 3 prime UTR variant | G/T | snv | 0.38 | 3 | ||||
| rs17690122 | 5 | 132532143 | intron variant | A/G;T | snv | 3 | |||||
| rs743562 | 5 | 132536691 | intron variant | C/T | snv | 0.35 | 3 |