Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77960347 | 18 | 49583585 | missense variant | A/C;G | snv | 4.0E-06; 8.7E-03 | 6 | ||||
rs11046205 | 12 | 21839392 | intron variant | G/A | snv | 0.19 | 2 | ||||
rs11265263 | 1 | 159740727 | intergenic variant | C/A;T | snv | 2 | |||||
rs17689882 | 17 | 45829462 | intron variant | G/A | snv | 0.14 | 2 | ||||
rs2175898 | 6 | 151875817 | intron variant | C/G;T | snv | 2 | |||||
rs228682 | 1 | 7796286 | intron variant | T/C | snv | 0.35 | 2 | ||||
rs10473984 | 5 | 76971301 | intron variant | G/T | snv | 0.12 | 1 | ||||
rs1080963 | 22 | 15376497 | intergenic variant | C/T | snv | 1 | |||||
rs12137927 | 1 | 7811169 | intron variant | T/C | snv | 0.20 | 1 | ||||
rs138191010 | 7 | 145416641 | intergenic variant | G/T | snv | 1 | |||||
rs1403522266 | 4 | 47320137 | missense variant | A/G | snv | 4.0E-06 | 1 | ||||
rs1475157 | 6 | 6016936 | intergenic variant | A/G | snv | 0.17 | 1 | ||||
rs2965087 | 7 | 103471538 | intron variant | T/C | snv | 0.45 | 1 | ||||
rs3756290 | 5 | 131616057 | intron variant | A/G | snv | 0.56 | 1 | ||||
rs4481363 | 5 | 165047713 | intron variant | C/A | snv | 0.55 | 1 | ||||
rs5440 | 12 | 6839735 | 3 prime UTR variant | A/G | snv | 0.56 | 1 | ||||
rs58682566 | 18 | 45951902 | intron variant | A/G | snv | 9.9E-02 | 1 | ||||
rs713224 | 4 | 186491213 | intron variant | G/A;C | snv | 1 | |||||
rs749865093 | 11 | 18029360 | missense variant | C/T | snv | 3.2E-05 | 1 | ||||
rs753009654 | 6 | 6002360 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||||
rs757522886 | 1 | 236885125 | missense variant | C/T | snv | 8.0E-06 | 1 | ||||
rs7582472 | 2 | 133887223 | regulatory region variant | T/C | snv | 0.21 | 1 | ||||
rs8836 | 17 | 76081416 | 3 prime UTR variant | G/A;C;T | snv | 1.6E-05; 0.54; 4.8E-05 | 1 | ||||
rs2535629 | 0.827 | 0.040 | 3 | 52799203 | intron variant | G/A;C | snv | 9 | |||
rs2239547 | 0.882 | 0.040 | 3 | 52821213 | intron variant | T/C | snv | 0.27 | 6 |