Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 38 | ||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 14 | ||
rs4820268 | 0.851 | 0.160 | 22 | 37073551 | missense variant | G/A;C | snv | 0.53; 4.0E-06 | 14 | ||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 11 | |||
rs4895441 | 0.925 | 0.080 | 6 | 135105435 | upstream gene variant | A/G | snv | 0.21 | 10 | ||
rs9376092 | 0.851 | 0.120 | 6 | 135106006 | upstream gene variant | C/A | snv | 0.24 | 10 | ||
rs129128 | 6 | 26125114 | intron variant | C/T | snv | 0.91 | 7 | ||||
rs7203560 | 1.000 | 0.080 | 16 | 134391 | intron variant | T/G | snv | 2.0E-02 | 7 | ||
rs12216125 | 0.925 | 0.120 | 6 | 25997230 | intron variant | C/T | snv | 0.26 | 6 | ||
rs837763 | 16 | 88787321 | upstream gene variant | C/G;T | snv | 5 | |||||
rs2213169 | 11 | 5281833 | intron variant | G/A;T | snv | 4.2E-02 | 4 | ||||
rs857725 | 1 | 158638145 | stop gained | T/A;G | snv | 4.0E-06; 0.28 | 3 | ||||
rs2160906 | 22 | 37097138 | intron variant | G/A | snv | 0.17 | 3 | ||||
rs1541252 | 1 | 203682799 | 5 prime UTR variant | T/A;C | snv | 2 | |||||
rs2266928 | 16 | 530124 | intron variant | C/A;G | snv | 2 | |||||
rs950488 | 1 | 158490185 | intron variant | C/A | snv | 0.19 | 2 | ||||
rs228904 | 22 | 37098774 | intron variant | A/G | snv | 0.17 | 2 | ||||
rs9937239 | 16 | 87073514 | downstream gene variant | G/A;C | snv | 1 |