| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs76481776 | 0.925 | 0.200 | 7 | 129770387 | non coding transcript exon variant | C/G;T | snv | 5.9E-02 | 4 | ||
| rs104894559 | 0.882 | 0.200 | 17 | 60150074 | missense variant | C/T | snv | 2.5E-04 | 1.4E-04 | 3 | |
| rs1805110 | 0.882 | 0.200 | 1 | 91861488 | missense variant | G/A | snv | 0.13 | 0.13 | 3 | |
| rs2489188 | 0.925 | 0.200 | 1 | 91866932 | intron variant | C/T | snv | 0.65 | 2 | ||
| rs2903908 | 0.925 | 0.200 | 20 | 46065308 | intron variant | T/C | snv | 0.22 | 2 | ||
| rs4936742 | 0.925 | 0.200 | 11 | 122770378 | intron variant | T/C | snv | 0.64 | 2 | ||
| rs76546355 | 0.925 | 0.200 | 6 | 31381371 | downstream gene variant | G/A | snv | 4.8E-02 | 2 | ||
| rs9517723 | 0.925 | 0.200 | 13 | 99432425 | non coding transcript exon variant | T/C | snv | 0.65 | 2 | ||
| rs10454134 | 1.000 | 0.200 | 2 | 48420887 | TF binding site variant | G/A | snv | 0.14 | 1 | ||
| rs104895083 | 0.925 | 0.200 | 16 | 3247166 | missense variant | G/C;T | snv | 4.0E-05; 1.2E-05 | 1 | ||
| rs1065407 | 1.000 | 0.200 | 5 | 96776379 | 3 prime UTR variant | T/A;G | snv | 3.3E-05; 0.26 | 1 | ||
| rs111874856 | 1.000 | 0.200 | 18 | 21028924 | missense variant | C/T | snv | 1 | |||
| rs112108028 | 1.000 | 0.200 | 18 | 20959861 | missense variant | G/A | snv | 1 | |||
| rs112130712 | 1.000 | 0.200 | 18 | 20967783 | missense variant | T/C | snv | 1 | |||
| rs11574944 | 1.000 | 0.200 | 16 | 30498669 | intron variant | C/T | snv | 0.25 | 1 | ||
| rs116799036 | 1.000 | 0.200 | 6 | 31381371 | downstream gene variant | G/A | snv | 1 | |||
| rs11769828 | 1.000 | 0.200 | 7 | 150534221 | intergenic variant | C/T | snv | 0.19 | 1 | ||
| rs12119179 | 0.925 | 0.200 | 1 | 67281732 | downstream gene variant | A/C | snv | 0.30 | 1 | ||
| rs12141431 | 1.000 | 0.200 | 1 | 67281340 | downstream gene variant | G/C | snv | 0.23 | 1 | ||
| rs13154629 | 1.000 | 0.200 | 5 | 96786754 | non coding transcript exon variant | C/T | snv | 0.16 | 1 | ||
| rs1327295035 | 1.000 | 0.200 | 6 | 52187730 | missense variant | A/G | snv | 1 | |||
| rs1462891 | 1.000 | 0.200 | 8 | 31973417 | intron variant | T/C | snv | 0.72 | 1 | ||
| rs149034313 | 1.000 | 0.200 | 22 | 31278338 | missense variant | C/G;T | snv | 6.4E-03; 1.2E-05 | 1 | ||
| rs1608157 | 1.000 | 0.200 | 7 | 150549936 | intergenic variant | C/G;T | snv | 1 | |||
| rs17633132 | 1.000 | 0.200 | 8 | 17642610 | splice region variant | C/G;T | snv | 8.0E-06; 0.11 | 1 |