| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10911362 | 1.000 | 0.040 | 1 | 183579857 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs10956514 | 1.000 | 0.040 | 8 | 130240512 | intron variant | A/G | snv | 0.37 | 1 | ||
| rs1101998 | 1.000 | 0.040 | 1 | 159029494 | intron variant | C/T | snv | 0.65 | 1 | ||
| rs11031728 | 1.000 | 0.040 | 11 | 32342070 | intron variant | C/G | snv | 0.18 | 1 | ||
| rs11040 | 1.000 | 0.040 | 6 | 81752132 | missense variant | C/A;G;T | snv | 1 | |||
| rs11117415 | 1.000 | 0.040 | 16 | 85917080 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs11246213 | 1.000 | 0.040 | 11 | 612967 | intron variant | A/G | snv | 0.25 | 0.33 | 1 | |
| rs11556887 | 1.000 | 0.040 | 2 | 230212961 | missense variant | G/A | snv | 0.10 | 7.4E-02 | 1 | |
| rs11567764 | 1.000 | 0.040 | 5 | 35873503 | missense variant | G/A;T | snv | 9.5E-03; 4.0E-06 | 1 | ||
| rs11774633 | 1.000 | 0.040 | 8 | 130177997 | intron variant | C/T | snv | 0.61 | 1 | ||
| rs1190662183 | 1.000 | 0.040 | 19 | 10338932 | synonymous variant | C/T | snv | 1 | |||
| rs11958933 | 1.000 | 0.040 | 5 | 25323598 | intron variant | G/A | snv | 0.70 | 1 | ||
| rs12294076 | 1.000 | 0.040 | 11 | 103256336 | intron variant | T/C | snv | 6.8E-02 | 1 | ||
| rs12297124 | 1.000 | 0.040 | 12 | 131920888 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs1242137541 | 1.000 | 0.040 | 10 | 17853040 | synonymous variant | C/T | snv | 7.0E-06 | 1 | ||
| rs12437118 | 1.000 | 0.040 | 14 | 76517387 | intron variant | G/A;C | snv | 1 | |||
| rs12456774 | 1.000 | 0.040 | 18 | 22592612 | intergenic variant | G/A | snv | 0.17 | 1 | ||
| rs12654043 | 1.000 | 0.040 | 5 | 150846533 | 5 prime UTR variant | A/C;G | snv | 1 | |||
| rs13389814 | 1.000 | 0.040 | 2 | 118984374 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs13422 | 1.000 | 0.040 | 17 | 15230858 | 3 prime UTR variant | T/G | snv | 0.53 | 0.57 | 1 | |
| rs142513793 | 1.000 | 0.040 | X | 48047088 | intron variant | C/T | snv | 2.1E-02 | 1 | ||
| rs1449626 | 1.000 | 0.040 | 11 | 47269208 | 5 prime UTR variant | A/C | snv | 0.26 | 1 | ||
| rs1449627 | 1.000 | 0.040 | 11 | 47269433 | 5 prime UTR variant | T/C;G | snv | 1 | |||
| rs1633256 | 1.000 | 0.040 | 1 | 159032767 | intron variant | A/G | snv | 0.70 | 1 | ||
| rs17175227 | 1.000 | 0.040 | 14 | 70035333 | downstream gene variant | G/A;C | snv | 2.1E-02 | 1 |