Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1453414 | 0.827 | 0.080 | 11 | 5807854 | intron variant | G/C;T | snv | 7 | |||
rs6021247 | 1.000 | 0.080 | 20 | 51492442 | intron variant | G/A | snv | 0.65 | 7 | ||
rs6547741 | 0.807 | 0.080 | 2 | 27633057 | intron variant | G/A | snv | 0.53 | 7 | ||
rs77452476 | 0.827 | 0.080 | 9 | 131087186 | intron variant | T/G | snv | 0.18 | 7 | ||
rs79767424 | 0.827 | 0.080 | 5 | 19108581 | intron variant | G/T | snv | 4.1E-02 | 7 | ||
rs10462706 | 0.827 | 0.080 | 5 | 1343679 | intron variant | C/T | snv | 0.14 | 6 | ||
rs10851478 | 0.827 | 0.080 | 15 | 49536822 | intron variant | T/C | snv | 0.30 | 6 | ||
rs1800628 | 0.827 | 0.080 | 6 | 31579073 | downstream gene variant | G/A | snv | 7.3E-02 | 6 | ||
rs2398180 | 0.827 | 0.080 | 15 | 96319940 | intron variant | C/T | snv | 0.62 | 6 | ||
rs3129780 | 0.827 | 0.080 | 6 | 32679924 | intergenic variant | T/A;C | snv | 6 | |||
rs928674 | 0.827 | 0.080 | 9 | 131076637 | intron variant | A/G | snv | 0.16 | 6 | ||
rs10090787 | 1.000 | 0.080 | 8 | 120798309 | intron variant | C/T | snv | 0.34 | 3 | ||
rs11545028 | 1.000 | 0.080 | 16 | 78099774 | 5 prime UTR variant | C/T | snv | 0.30 | 0.28 | 3 | |
rs2046463 | 1.000 | 0.080 | 4 | 176681548 | intron variant | G/A;C | snv | 3 | |||
rs9849237 | 1.000 | 0.080 | 3 | 2633505 | intron variant | C/T | snv | 0.25 | 3 | ||
rs9862 | 1.000 | 0.080 | 22 | 32857293 | missense variant | T/A;C | snv | 4.0E-06; 0.55 | 3 | ||
rs1045487 | 1.000 | 0.080 | 2 | 201284973 | synonymous variant | G/A | snv | 9.5E-02 | 0.10 | 2 | |
rs11130760 | 1.000 | 0.080 | 3 | 60210809 | intron variant | G/T | snv | 0.12 | 2 | ||
rs1473418 | 1.000 | 0.080 | 18 | 63319316 | 5 prime UTR variant | C/G | snv | 0.98 | 2 | ||
rs17071138 | 1.000 | 0.080 | 18 | 63476675 | upstream gene variant | T/C | snv | 2.9E-02 | 2 | ||
rs1950252 | 1.000 | 0.080 | 14 | 23309489 | 3 prime UTR variant | A/G | snv | 0.93 | 2 | ||
rs2040639 | 1.000 | 0.080 | 7 | 152678103 | upstream gene variant | T/C;G | snv | 2 | |||
rs2292566 | 1.000 | 0.080 | 1 | 225831952 | synonymous variant | G/A | snv | 2 | |||
rs3092904 | 1.000 | 0.080 | 13 | 48477345 | intron variant | T/A | snv | 0.24 | 0.20 | 2 | |
rs33438 | 1.000 | 0.080 | 19 | 30454165 | intron variant | G/A | snv | 0.50 | 2 |