Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
rs1141718 | 0.724 | 0.280 | 6 | 159688224 | missense variant | A/G | snv | 15 | |||
rs4987023 | 0.807 | 0.120 | 6 | 159692661 | missense variant | C/T | snv | 7.0E-06 | 6 | ||
rs5746136 | 0.807 | 0.200 | 6 | 159682052 | 3 prime UTR variant | C/T | snv | 0.27 | 6 | ||
rs781598341 | 0.827 | 0.240 | 6 | 159682510 | missense variant | T/C | snv | 4.0E-06 | 5 | ||
rs6917589 | 0.882 | 0.120 | 6 | 159678228 | 3 prime UTR variant | T/C | snv | 0.22 | 3 | ||
rs11575993 | 0.925 | 0.040 | 6 | 159688219 | missense variant | G/A | snv | 2 | |||
rs1165109290 | 0.925 | 0.080 | 6 | 159692850 | synonymous variant | G/A | snv | 4.2E-06 | 2 | ||
rs1261281771 | 0.925 | 0.080 | 6 | 159688191 | missense variant | C/G | snv | 7.0E-06 | 2 | ||
rs2758330 | 0.925 | 0.080 | 6 | 159683812 | intron variant | G/T | snv | 0.77 | 2 | ||
rs2758331 | 0.925 | 0.080 | 6 | 159684038 | intron variant | C/A | snv | 0.40 | 2 | ||
rs2758339 | 0.925 | 0.080 | 6 | 159691552 | 3 prime UTR variant | A/C;T | snv | 2 | |||
rs2842958 | 0.925 | 0.080 | 6 | 159687393 | intron variant | A/G | snv | 0.77 | 2 | ||
rs370671213 | 0.925 | 0.080 | 6 | 159692722 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 2 | ||
rs748423903 | 0.925 | 0.080 | 6 | 159688144 | missense variant | C/G;T | snv | 8.0E-06 | 2 | ||
rs779731636 | 0.925 | 0.120 | 6 | 159685026 | missense variant | C/A | snv | 8.6E-06 | 2 | ||
rs1019827482 | 1.000 | 6 | 159692550 | missense variant | T/C | snv | 6.0E-06 | 1 | |||
rs1176281575 | 1.000 | 0.040 | 6 | 159684905 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1264525329 | 1.000 | 0.120 | 6 | 159682587 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs1336268032 | 1.000 | 0.040 | 6 | 159692718 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
rs1419367513 | 6 | 159762678 | non coding transcript exon variant | G/A | snv | 1 | |||||
rs1799725 | 6 | 159692840 | missense variant | A/G | snv | 1 | |||||
rs2842980 | 1.000 | 0.040 | 6 | 159679084 | 3 prime UTR variant | A/T | snv | 0.77 | 1 | ||
rs4342445 | 6 | 159677190 | 3 prime UTR variant | G/A | snv | 0.22 | 1 |