Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10255208 | 0.925 | 0.160 | 7 | 36819038 | non coding transcript exon variant | A/G | snv | 0.46 | 2 | ||
rs1044498 | 0.752 | 0.360 | 6 | 131851228 | missense variant | A/C;G | snv | 0.19 | 15 | ||
rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
rs1063537 | 0.807 | 0.320 | 3 | 186856286 | 3 prime UTR variant | C/T | snv | 9.6E-02 | 6 | ||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs10823108 | 0.925 | 0.160 | 10 | 67900736 | intron variant | G/A | snv | 7.1E-02 | 2 | ||
rs1136410 | 0.559 | 0.760 | 1 | 226367601 | missense variant | A/G | snv | 0.21 | 0.15 | 70 | |
rs1137933 | 0.882 | 0.160 | 17 | 27778906 | synonymous variant | G/A | snv | 0.20 | 0.21 | 4 | |
rs11549465 | 0.597 | 0.680 | 14 | 61740839 | missense variant | C/T | snv | 8.8E-02 | 7.7E-02 | 55 | |
rs11643718 | 0.807 | 0.240 | 16 | 56899607 | missense variant | G/A | snv | 0.11 | 8.4E-02 | 10 | |
rs11646213 | 0.827 | 0.320 | 16 | 82609046 | intergenic variant | A/T | snv | 0.47 | 6 | ||
rs11771443 | 0.790 | 0.360 | 7 | 150990599 | upstream gene variant | C/T | snv | 0.16 | 8 | ||
rs117897666 | 0.882 | 0.160 | 15 | 73811619 | intergenic variant | C/T | snv | 3 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs1332629192 | 0.851 | 0.200 | 4 | 73404374 | missense variant | C/T | snv | 7 | |||
rs136161 | 0.925 | 0.160 | 22 | 36261386 | intron variant | G/C | snv | 0.51 | 3 | ||
rs1400094618 | 0.882 | 0.240 | 14 | 102229508 | missense variant | A/G | snv | 3 | |||
rs1411766 | 0.882 | 0.160 | 13 | 109599813 | intron variant | G/A;T | snv | 3 | |||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs14259 | 0.724 | 0.360 | 12 | 121915890 | missense variant | A/C;G | snv | 4.0E-06; 0.32 | 19 | ||
rs143101792 | 0.851 | 0.320 | 1 | 159714026 | stop gained | G/C | snv | 8.8E-05 | 1.3E-04 | 5 | |
rs1501299 | 0.597 | 0.720 | 3 | 186853334 | intron variant | G/C;T | snv | 52 | |||
rs1531343 | 0.925 | 0.160 | 12 | 65781114 | intron variant | G/C;T | snv | 2 | |||
rs16139 | 0.658 | 0.560 | 7 | 24285260 | missense variant | T/A;C | snv | 4.0E-06; 3.0E-02 | 36 |