| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12800438 | 1.000 | 0.080 | 11 | 71459957 | non coding transcript exon variant | G/A;T | snv | 5 | |||
| rs10485505 | 1.000 | 0.080 | 20 | 34437762 | intron variant | C/G;T | snv | 3 | |||
| rs10519613 | 1.000 | 0.080 | 4 | 141732931 | 3 prime UTR variant | C/A | snv | 0.10 | 3 | ||
| rs10836347 | 1.000 | 0.080 | 11 | 35231586 | 3 prime UTR variant | C/T | snv | 0.11 | 3 | ||
| rs157077 | 1.000 | 0.080 | 10 | 104278136 | intron variant | T/C | snv | 0.45 | 0.53 | 3 | |
| rs171915 | 1.000 | 0.080 | 6 | 142545708 | intron variant | G/A | snv | 0.22 | 3 | ||
| rs2830581 | 1.000 | 0.080 | 21 | 26921481 | 3 prime UTR variant | G/A;C | snv | 3 | |||
| rs6940552 | 1.000 | 0.080 | 6 | 30044563 | intron variant | G/A | snv | 0.12 | 3 | ||
| rs750814369 | 1.000 | 0.080 | 11 | 65570617 | missense variant | C/A;T | snv | 2.8E-05 | 3 | ||
| rs80291436 | 1.000 | 0.080 | X | 7843706 | missense variant | T/A;C;G | snv | 4.9E-05; 0.19 | 3 | ||
| rs886039463 | 1.000 | 0.080 | 12 | 112489096 | missense variant | C/A | snv | 3 | |||
| rs1014509103 | 1.000 | 0.080 | 1 | 161194005 | missense variant | G/A | snv | 4.0E-06 | 2.8E-05 | 2 | |
| rs1053133 | 1.000 | 0.080 | 6 | 41932887 | 3 prime UTR variant | C/A;T | snv | 2 | |||
| rs1065205 | 1.000 | 0.080 | 18 | 63655761 | missense variant | T/C;G | snv | 0.15 | 2 | ||
| rs12427129 | 1.000 | 0.080 | 12 | 53973906 | missense variant | C/T | snv | 9.0E-02 | 7.0E-02 | 2 | |
| rs12438080 | 1.000 | 0.080 | 15 | 100541858 | intron variant | A/C | snv | 0.50 | 2 | ||
| rs17084733 | 1.000 | 0.080 | 4 | 54738774 | 3 prime UTR variant | G/A | snv | 0.10 | 2 | ||
| rs1713449 | 1.000 | 0.080 | 14 | 20373548 | missense variant | C/T | snv | 0.26 | 0.29 | 2 | |
| rs17501292 | 1.000 | 0.080 | 7 | 27201854 | non coding transcript exon variant | T/C;G | snv | 2 | |||
| rs2118593 | 1.000 | 0.080 | 3 | 72447740 | upstream gene variant | G/A;C;T | snv | 2 | |||
| rs2118610 | 1.000 | 0.080 | 15 | 67135996 | intron variant | T/C | snv | 0.59 | 2 | ||
| rs2148356 | 1.000 | 0.080 | 9 | 7395038 | intergenic variant | G/A;C | snv | 2 | |||
| rs2276724 | 1.000 | 0.080 | 3 | 126135566 | missense variant | T/C | snv | 0.14 | 0.15 | 2 | |
| rs2280235 | 1.000 | 0.080 | 2 | 190979104 | splice region variant | A/G | snv | 0.23 | 2 | ||
| rs28599926 | 1.000 | 0.080 | 15 | 22225320 | mature miRNA variant | C/T | snv | 4.8E-02 | 0.14 | 2 |