| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10052957 | 0.851 | 0.160 | 5 | 143407136 | non coding transcript exon variant | G/A | snv | 0.28 | 4 | ||
| rs1008438 | 0.807 | 0.120 | 6 | 31815431 | upstream gene variant | A/C;T | snv | 6 | |||
| rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
| rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
| rs1042718 | 0.925 | 0.080 | 5 | 148827354 | missense variant | C/A;T | snv | 0.23; 4.0E-06 | 3 | ||
| rs1043618 | 0.752 | 0.280 | 6 | 31815730 | 5 prime UTR variant | G/A;C;T | snv | 0.39; 2.0E-05; 4.0E-06 | 10 | ||
| rs1061581 | 0.827 | 0.200 | 6 | 31816809 | synonymous variant | G/A | snv | 6 | |||
| rs11896604 | 0.776 | 0.200 | 2 | 54252062 | intron variant | C/A;G;T | snv | 8 | |||
| rs12615793 | 0.851 | 0.280 | 2 | 54248777 | intron variant | G/A;T | snv | 4 | |||
| rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
| rs130293 | 1.000 | 0.040 | 22 | 32825953 | intron variant | G/A | snv | 0.92 | 1 | ||
| rs157928 | 1.000 | 0.040 | 7 | 130896599 | intron variant | T/C | snv | 0.29 | 1 | ||
| rs17045754 | 0.790 | 0.280 | 2 | 54269620 | intron variant | G/A;C | snv | 7 | |||
| rs1799889 | 0.649 | 0.600 | 7 | 101126430 | upstream gene variant | A/G | snv | 31 | |||
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
| rs1962430 | 1.000 | 0.040 | 8 | 9902110 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
| rs1965708 | 0.851 | 0.200 | 10 | 79557289 | missense variant | G/T | snv | 0.22 | 0.25 | 6 | |
| rs199983 | 1.000 | 0.040 | 6 | 104412396 | intergenic variant | A/G | snv | 0.52 | 1 | ||
| rs2070951 | 0.776 | 0.320 | 4 | 148436862 | splice region variant | G/A;C | snv | 4.2E-06; 0.53 | 9 | ||
| rs2072472 | 0.732 | 0.200 | 2 | 102026557 | intron variant | A/G | snv | 0.24 | 13 | ||
| rs2227956 | 0.752 | 0.400 | 6 | 31810495 | missense variant | G/A;C;T | snv | 0.87 | 12 | ||
| rs2272026 | 1.000 | 0.040 | 8 | 9900090 | non coding transcript exon variant | C/G;T | snv | 1 | |||
| rs2297441 | 0.807 | 0.160 | 20 | 63696229 | 3 prime UTR variant | G/A;C | snv | 6 | |||
| rs2918417 | 1.000 | 0.040 | 5 | 143346605 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs33388 | 0.776 | 0.360 | 5 | 143317730 | intron variant | A/T | snv | 0.53 | 12 |