Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10038095 | 5 | 75341886 | intron variant | A/T | snv | 0.38 | 2 | ||||
rs10045497 | 5 | 75340659 | intron variant | C/A | snv | 0.35 | 2 | ||||
rs10054063 | 5 | 173965395 | downstream gene variant | A/T | snv | 0.26 | 4 | ||||
rs10066168 | 5 | 157057207 | intron variant | C/G;T | snv | 2 | |||||
rs10102164 | 8 | 54509054 | upstream gene variant | G/A | snv | 0.19 | 3 | ||||
rs10104003 | 8 | 54509880 | intron variant | C/T | snv | 0.19 | 1 | ||||
rs10128711 | 11 | 18611437 | intron variant | T/C | snv | 0.64 | 0.55 | 2 | |||
rs1014283 | 7 | 87447271 | intron variant | C/A;T | snv | 2 | |||||
rs1016988 | 5 | 132408882 | upstream gene variant | T/C | snv | 0.20 | 2 | ||||
rs10172650 | 2 | 20982585 | intergenic variant | G/A | snv | 0.28 | 2 | ||||
rs10176901 | 2 | 168974151 | intron variant | G/A | snv | 0.57 | 2 | ||||
rs10185855 | 2 | 101025798 | intron variant | A/G | snv | 0.35 | 4 | ||||
rs10199768 | 2 | 21021128 | intron variant | G/T | snv | 0.35 | 1 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs10260606 | 7 | 44544952 | upstream gene variant | G/A;C | snv | 2 | |||||
rs10275712 | 7 | 1043282 | intron variant | G/A | snv | 0.18 | 1 | ||||
rs1030431 | 8 | 58399138 | intergenic variant | A/G;T | snv | 3 | |||||
rs1038026 | 1.000 | 0.080 | 19 | 44901805 | 3 prime UTR variant | A/G;T | snv | 3 | |||
rs10401969 | 0.776 | 0.240 | 19 | 19296909 | intron variant | T/C | snv | 0.10 | 22 | ||
rs10402271 | 1.000 | 0.080 | 19 | 44825957 | downstream gene variant | T/G | snv | 0.28 | 4 | ||
rs10408163 | 19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 | 6 | ||||
rs1041968 | 2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 | 4 | |||
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 6 | |
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 10 | ||
rs10460181 | 19 | 44636865 | intron variant | A/G;T | snv | 0.26 | 2 |