Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1000879 | 2 | 218439407 | intron variant | G/A | snv | 4.1E-02 | 3 | ||||
rs10096633 | 1.000 | 0.040 | 8 | 19973410 | regulatory region variant | C/T | snv | 0.22 | 7 | ||
rs10120653 | 9 | 134415237 | intron variant | G/T | snv | 1.2E-02 | 3 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 16 | ||
rs1031045 | 8 | 19943601 | intron variant | G/A | snv | 0.12 | 3 | ||||
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 11 | ||
rs10503669 | 0.925 | 0.080 | 8 | 19990179 | intergenic variant | C/A | snv | 8.4E-02 | 8 | ||
rs1051921 | 0.925 | 0.120 | 7 | 73593613 | 3 prime UTR variant | G/A | snv | 0.15 | 8 | ||
rs1059507 | 1.000 | 0.080 | 8 | 19966452 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
rs10750097 | 1.000 | 0.040 | 11 | 116793324 | upstream gene variant | G/A;C | snv | 5 | |||
rs1077835 | 15 | 58431227 | intron variant | A/G | snv | 0.34 | 5 | ||||
rs10808546 | 8 | 125483576 | intron variant | C/T | snv | 0.39 | 7 | ||||
rs11216126 | 1.000 | 0.040 | 11 | 116746524 | downstream gene variant | A/C | snv | 0.11 | 4 | ||
rs11216162 | 11 | 116857561 | non coding transcript exon variant | G/A | snv | 0.17 | 3 | ||||
rs1121980 | 0.807 | 0.240 | 16 | 53775335 | intron variant | G/A;C | snv | 11 | |||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 7 | ||||
rs11568746 | 9 | 99105926 | intron variant | C/G | snv | 2.1E-05 | 6 | ||||
rs11570892 | 8 | 19966106 | 3 prime UTR variant | A/G;T | snv | 3 | |||||
rs11571111 | 1 | 204161105 | intron variant | C/A | snv | 5.0E-03 | 4 | ||||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs11613352 | 0.827 | 0.160 | 12 | 57398797 | intron variant | C/T | snv | 0.19 | 6 | ||
rs11824953 | 11 | 102949239 | intron variant | C/G | snv | 2.7E-02 | 3 | ||||
rs11828157 | 11 | 102947395 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs11856159 | 15 | 58406811 | intron variant | C/A;G;T | snv | 4 | |||||
rs11902417 | 2 | 20976028 | intergenic variant | G/A | snv | 0.25 | 7 |