Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 83 | ||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 28 | ||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 15 | |||||
rs7137828 | 0.763 | 0.200 | 12 | 111494996 | intron variant | C/A;T | snv | 15 | |||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 11 | |||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 10 | |||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 10 | |||
rs2681492 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 10 | |||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 10 | |||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 | |||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs2071410 | 0.882 | 0.160 | 15 | 90877710 | intron variant | C/A;G;T | snv | 7 | |||
rs1290784 | 3 | 169379112 | intron variant | C/A;T | snv | 6 | |||||
rs13149993 | 4 | 80237391 | regulatory region variant | G/A;C | snv | 6 | |||||
rs1495743 | 8 | 18415790 | intergenic variant | G/A;C | snv | 6 | |||||
rs17035646 | 1 | 10736490 | intron variant | G/A;T | snv | 6 | |||||
rs2156552 | 1.000 | 0.040 | 18 | 49655298 | downstream gene variant | A/G;T | snv | 6 | |||
rs9292468 | 5 | 32818967 | intergenic variant | T/A;C | snv | 6 | |||||
rs10184428 | 2 | 164155317 | intron variant | C/A;G | snv | 5 | |||||
rs12978472 | 19 | 7257979 | intron variant | C/G;T | snv | 5 | |||||
rs2004776 | 1 | 230712956 | intron variant | C/G;T | snv | 5 | |||||
rs2013002 | 12 | 111762346 | intron variant | T/A;C | snv | 5 | |||||
rs2304128 | 19 | 19635342 | intron variant | G/C;T | snv | 5 | |||||
rs4722551 | 7 | 25952206 | upstream gene variant | T/C;G | snv | 5 |