Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs876658657 | 0.677 | 0.280 | 3 | 37020356 | missense variant | A/G | snv | 4.0E-06 | 25 | ||
rs140693 | 0.763 | 0.280 | 3 | 129436608 | missense variant | C/T | snv | 5.8E-02 | 3.1E-02 | 10 | |
rs10937405 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 9 | ||
rs577715207 | 0.827 | 0.160 | 3 | 189886413 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 8 | |
rs2229090 | 0.827 | 0.160 | 3 | 14145845 | 3 prime UTR variant | G/C | snv | 0.25 | 0.22 | 6 | |
rs181696 | 0.925 | 0.080 | 3 | 155548315 | intron variant | T/C | snv | 0.55 | 3 | ||
rs143752852 | 3 | 49902723 | missense variant | A/G | snv | 8.8E-05 | 5.6E-05 | 1 | |||
rs17429138 | 3 | 189527804 | intergenic variant | A/G | snv | 0.26 | 1 | ||||
rs4396880 | 3 | 189638432 | intron variant | G/A | snv | 0.34 | 1 | ||||
rs3114020 | 0.882 | 0.200 | 4 | 88162514 | intron variant | T/C | snv | 0.40 | 5 | ||
rs1397529 | 0.882 | 0.080 | 4 | 143471009 | 3 prime UTR variant | A/C;T | snv | 4 | |||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs2736100 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 83 | ||
rs3212227 | 0.566 | 0.840 | 5 | 159315942 | 3 prime UTR variant | T/G | snv | 0.26 | 65 | ||
rs2736098 | 0.600 | 0.600 | 5 | 1293971 | synonymous variant | C/T | snv | 0.29 | 0.22 | 48 | |
rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 42 | ||
rs2853669 | 0.649 | 0.320 | 5 | 1295234 | upstream gene variant | A/G | snv | 0.25 | 35 | ||
rs2853676 | 0.667 | 0.560 | 5 | 1288432 | intron variant | T/A;C | snv | 29 | |||
rs11134527 | 0.677 | 0.400 | 5 | 168768351 | intron variant | G/A | snv | 0.25 | 24 | ||
rs2853677 | 0.724 | 0.240 | 5 | 1287079 | 3 prime UTR variant | G/A | snv | 0.63 | 19 | ||
rs402710 | 0.716 | 0.320 | 5 | 1320607 | non coding transcript exon variant | C/T | snv | 0.33 | 0.38 | 18 | |
rs4975616 | 0.763 | 0.320 | 5 | 1315545 | downstream gene variant | G/A | snv | 0.51 | 12 | ||
rs61748181 | 0.827 | 0.120 | 5 | 1294051 | missense variant | C/T | snv | 2.2E-02 | 2.2E-02 | 10 | |
rs112290073 | 0.882 | 0.080 | 5 | 1285917 | intron variant | G/A | snv | 7.8E-03 | 4 | ||
rs138895564 | 0.882 | 0.080 | 5 | 1271959 | intron variant | C/T | snv | 5.1E-03 | 4 |