Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1339638227 | 0.925 | 0.120 | 9 | 21971119 | missense variant | T/C | snv | 4.3E-06 | 2 | ||
rs6475609 | 0.925 | 0.120 | 9 | 22106272 | intron variant | A/C;G;T | snv | 2 | |||
rs488087 | 0.925 | 0.120 | 9 | 133071212 | synonymous variant | C/A;T | snv | 0.11 | 0.26 | 2 | |
rs2236479 | 0.925 | 0.160 | 21 | 45499218 | intron variant | G/A | snv | 0.40 | 2 | ||
rs747601652 | 0.925 | 0.120 | 1 | 74723233 | missense variant | A/G | snv | 1.2E-05 | 2 | ||
rs1810205 | 0.925 | 0.120 | 10 | 16923228 | intron variant | A/G | snv | 0.47 | 2 | ||
rs6127119 | 0.925 | 0.120 | 20 | 54162543 | intron variant | C/T | snv | 0.24 | 2 | ||
rs6464375 | 0.925 | 0.120 | 7 | 153928758 | intron variant | C/T | snv | 6.7E-02 | 2 | ||
rs876661110 | 0.925 | 0.120 | 2 | 47791093 | missense variant | G/A | snv | 2 | |||
rs7993418 | 0.925 | 0.120 | 13 | 28308924 | synonymous variant | G/A | snv | 0.80 | 0.67 | 2 | |
rs371609024 | 0.925 | 0.120 | 14 | 65629530 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
rs199474357 | 0.925 | 0.120 | 6 | 29942790 | missense variant | T/C;G | snv | 2 | |||
rs4795218 | 0.925 | 0.120 | 17 | 37718512 | intron variant | A/G | snv | 0.82 | 2 | ||
rs200349340 | 0.925 | 0.120 | 12 | 53962704 | non coding transcript exon variant | T/A;G | snv | 2 | |||
rs201753355 | 0.925 | 0.120 | 6 | 3019647 | missense variant | G/A;C | snv | 2.0E-05 | 2 | ||
rs13303010 | 0.925 | 0.120 | 1 | 959193 | intron variant | G/A | snv | 0.82 | 0.69 | 2 | |
rs12456874 | 0.925 | 0.120 | 18 | 13366863 | intron variant | A/G | snv | 0.20 | 2 | ||
rs1455311 | 0.925 | 0.160 | 4 | 79043433 | intron variant | A/G | snv | 0.14 | 2 | ||
rs1318 | 0.925 | 0.120 | 17 | 67695266 | 3 prime UTR variant | A/G | snv | 0.30 | 2 | ||
rs1810636 | 0.925 | 0.160 | 20 | 2674279 | regulatory region variant | A/C;T | snv | 2 | |||
rs1547374 | 0.925 | 0.120 | 21 | 42358786 | downstream gene variant | A/G | snv | 0.32 | 2 | ||
rs782095550 | 0.925 | 0.120 | 3 | 51386267 | missense variant | T/C | snv | 2 | |||
rs12939944 | 0.925 | 0.120 | 17 | 12056502 | intron variant | C/T | snv | 0.45 | 2 | ||
rs141095230 | 0.925 | 0.120 | 10 | 129536277 | missense variant | C/A;T | snv | 8.0E-06; 5.2E-05 | 2 | ||
rs3021088 | 0.925 | 0.120 | MT | 5460 | missense variant | G/A | snv | 2 |