Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10051330 | 5 | 158392616 | intron variant | A/G;T | snv | 2 | |||||
rs10092965 | 8 | 8515975 | intergenic variant | A/G | snv | 0.43 | 2 | ||||
rs10184428 | 2 | 164155317 | intron variant | C/A;G | snv | 5 | |||||
rs10255839 | 7 | 27249498 | intron variant | G/A | snv | 0.87 | 6 | ||||
rs10750766 | 11 | 65706327 | regulatory region variant | C/A | snv | 0.60 | 4 | ||||
rs10897164 | 11 | 61510303 | 3 prime UTR variant | A/G | snv | 0.13 | 3 | ||||
rs11065979 | 0.851 | 0.200 | 12 | 111621753 | intergenic variant | C/T | snv | 0.30 | 12 | ||
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 27 | ||
rs11099097 | 4 | 80246155 | intergenic variant | C/T | snv | 0.30 | 6 | ||||
rs11105352 | 12 | 89632685 | intron variant | G/A | snv | 0.14 | 4 | ||||
rs111478946 | 12 | 89665065 | intron variant | G/A | snv | 0.14 | 4 | ||||
rs112640876 | 11 | 1873813 | intron variant | A/G;T | snv | 3 | |||||
rs11513729 | 1.000 | 0.080 | 12 | 111835695 | downstream gene variant | C/T | snv | 0.29 | 5 | ||
rs11725969 | 4 | 155705436 | intron variant | C/T | snv | 0.24 | 5 | ||||
rs11731886 | 4 | 155738667 | downstream gene variant | A/C | snv | 0.21 | 3 | ||||
rs11781008 | 8 | 9295729 | intron variant | G/C;T | snv | 2 | |||||
rs12050759 | 15 | 74972850 | intron variant | G/A | snv | 0.27 | 2 | ||||
rs12080886 | 1 | 243222734 | intron variant | T/A;C | snv | 2 | |||||
rs12118370 | 1 | 112605645 | intron variant | A/G | snv | 0.24 | 3 | ||||
rs12194642 | 6 | 78829074 | intergenic variant | G/A | snv | 0.32 | 2 | ||||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs12579302 | 0.851 | 0.120 | 12 | 89656726 | intron variant | A/G | snv | 0.15 | 19 | ||
rs1275984 | 2 | 26688641 | upstream gene variant | A/C;G | snv | 4 | |||||
rs1275985 | 2 | 26688877 | upstream gene variant | C/T | snv | 0.50 | 3 | ||||
rs12799126 | 11 | 16286917 | intron variant | G/T | snv | 0.17 | 3 |