Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 12 | ||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs10857147 | 1.000 | 0.040 | 4 | 80259918 | intergenic variant | A/T | snv | 0.25 | 9 | ||
rs3918226 | 0.925 | 0.080 | 7 | 150993088 | intron variant | C/T | snv | 5.7E-02 | 9 | ||
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 8 | ||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs16998073 | 0.925 | 0.120 | 4 | 80263187 | upstream gene variant | A/G;T | snv | 7 | |||
rs77924615 | 1.000 | 0.080 | 16 | 20381010 | intron variant | G/A | snv | 0.16 | 7 | ||
rs1458038 | 0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 | 6 | ||
rs2823139 | 1.000 | 0.080 | 21 | 15204463 | intron variant | G/A | snv | 0.34 | 5 | ||
rs7832708 | 8 | 10332530 | intron variant | C/T | snv | 0.49 | 4 | ||||
rs10254101 | 7 | 151718450 | intron variant | C/T | snv | 0.23 | 3 | ||||
rs2290263 | 7 | 25847658 | intergenic variant | G/A | snv | 0.77 | 3 | ||||
rs11636251 | 15 | 75946679 | intron variant | C/T | snv | 0.42 | 2 | ||||
rs72683923 | 14 | 50269229 | synonymous variant | T/C | snv | 1.0E-02 | 9.9E-03 | 2 |