| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10969913 | 1.000 | 0.080 | 9 | 30866810 | intergenic variant | A/G | snv | 6.3E-02 | 3 | ||
| rs11122573 | 1.000 | 0.080 | 1 | 230701434 | upstream gene variant | C/T | snv | 8.0E-02 | 3 | ||
| rs17055178 | 1.000 | 0.080 | 5 | 157976402 | downstream gene variant | A/G | snv | 7.2E-02 | 3 | ||
| rs11055034 | 1.000 | 0.080 | 12 | 12737692 | intron variant | C/A;T | snv | 2 | |||
| rs17779457 | 1.000 | 0.080 | 9 | 27488094 | intron variant | T/A;G | snv | 2 | |||
| rs2238776 | 1.000 | 0.080 | 22 | 19770369 | intron variant | G/A;T | snv | 2 | |||
| rs56232506 | 1.000 | 0.080 | 7 | 47397647 | intron variant | G/A | snv | 0.35 | 2 | ||
| rs72915971 | 1.000 | 0.080 | 11 | 57158067 | intergenic variant | C/G | snv | 2.4E-02 | 2 | ||
| rs10009409 | 1.000 | 0.080 | 4 | 72989536 | intergenic variant | C/T | snv | 0.35 | 1 | ||
| rs1004030 | 1.000 | 0.080 | 14 | 22836440 | upstream gene variant | T/C | snv | 0.39 | 1 | ||
| rs10086908 | 1.000 | 0.080 | 8 | 126999692 | intron variant | T/C | snv | 0.28 | 1 | ||
| rs10122495 | 1.000 | 0.080 | 9 | 34049781 | upstream gene variant | T/A | snv | 0.73 | 1 | ||
| rs1016342 | 1.000 | 0.080 | 8 | 127080210 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs1031588 | 1.000 | 0.080 | 8 | 127081032 | non coding transcript exon variant | C/A | snv | 0.24 | 1 | ||
| rs1041449 | 1.000 | 0.080 | 21 | 41529494 | intron variant | A/G | snv | 0.42 | 1 | ||
| rs10460109 | 1.000 | 0.080 | 18 | 75324210 | intergenic variant | T/C | snv | 0.61 | 1 | ||
| rs1048169 | 1.000 | 0.080 | 9 | 19055967 | 3 prime UTR variant | T/C | snv | 0.46 | 1 | ||
| rs10763567 | 1.000 | 0.080 | 10 | 46057653 | regulatory region variant | G/A;T | snv | 1 | |||
| rs10774740 | 1.000 | 0.080 | 12 | 114228397 | intergenic variant | G/A;T | snv | 1 | |||
| rs10793821 | 1.000 | 0.080 | 5 | 134500518 | upstream gene variant | C/A;T | snv | 0.62 | 1 | ||
| rs10845938 | 1.000 | 0.080 | 12 | 14263984 | intergenic variant | A/G | snv | 0.52 | 1 | ||
| rs11125927 | 1.000 | 0.080 | 2 | 62525840 | regulatory region variant | G/A | snv | 0.86 | 1 | ||
| rs111599055 | 1.000 | 0.080 | 12 | 132563775 | intron variant | A/C;G | snv | 1 | |||
| rs11214775 | 1.000 | 0.080 | 11 | 113936459 | intron variant | G/A | snv | 0.29 | 1 | ||
| rs112193369 | 1.000 | 0.080 | 1 | 7498191 | intron variant | -/AGTGTG;AGTGTGTG;AGTGTTGGTG;AGTGTTGGTGTG;AGTGTTGGTGTGTG;GGTG | delins | 1 |