Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9973676 | 1.000 | 0.080 | 2 | 230954091 | intron variant | G/A | snv | 5.8E-02 | 2 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs9641609 | 1.000 | 0.080 | 7 | 118657790 | regulatory region variant | A/G | snv | 0.38 | 2 | ||
rs9632885 | 1.000 | 0.040 | 9 | 22072639 | intron variant | G/A | snv | 0.56 | 2 | ||
rs9632884 | 0.851 | 0.160 | 9 | 22072302 | intron variant | G/A;C | snv | 6 | |||
rs944801 | 0.882 | 0.120 | 9 | 22051671 | intron variant | G/A;C | snv | 4 | |||
rs944799 | 1.000 | 0.040 | 9 | 22050614 | intron variant | A/G | snv | 0.50 | 2 | ||
rs944797 | 0.882 | 0.120 | 9 | 22115287 | intron variant | T/C;G | snv | 0.49 | 5 | ||
rs9384331 | 1.000 | 0.080 | 6 | 150279905 | intergenic variant | T/C | snv | 0.12 | 2 | ||
rs9349379 | 0.732 | 0.200 | 6 | 12903725 | intron variant | A/G | snv | 0.32 | 19 | ||
rs91 | 1.000 | 0.080 | 7 | 24409992 | intron variant | T/C | snv | 0.41 | 2 | ||
rs8181050 | 1.000 | 0.040 | 9 | 22064392 | intron variant | G/A;C;T | snv | 2 | |||
rs8134546 | 1.000 | 0.080 | 21 | 34782568 | intron variant | T/C | snv | 8.7E-02 | 2 | ||
rs8089491 | 18 | 31763291 | upstream gene variant | G/A | snv | 5.4E-02 | 1 | ||||
rs7866783 | 1.000 | 0.040 | 9 | 22056360 | non coding transcript exon variant | A/G | snv | 0.71 | 2 | ||
rs7865618 | 0.776 | 0.240 | 9 | 22031006 | non coding transcript exon variant | G/A;T | snv | 11 | |||
rs7859727 | 1.000 | 0.080 | 9 | 22102166 | intron variant | C/T | snv | 0.57 | 3 | ||
rs7859362 | 9 | 22105928 | intron variant | T/C | snv | 0.64 | 2 | ||||
rs7857345 | 0.925 | 0.080 | 9 | 22087474 | non coding transcript exon variant | T/A;C | snv | 4 | |||
rs7857118 | 9 | 22124141 | intron variant | A/T | snv | 0.64 | 1 | ||||
rs7804216 | 1.000 | 0.080 | 7 | 149941248 | intergenic variant | C/G | snv | 0.24 | 2 | ||
rs77934287 | 1.000 | 0.080 | 12 | 23071319 | intron variant | A/G;T | snv | 2 | |||
rs77757620 | 1.000 | 0.080 | 15 | 42661399 | intron variant | C/T | snv | 3.8E-02 | 2 | ||
rs7689240 | 1.000 | 0.080 | 4 | 35313869 | intergenic variant | A/G | snv | 0.21 | 2 | ||
rs76294234 | 1.000 | 0.080 | 4 | 83241025 | intron variant | A/G | snv | 1.5E-02 | 2 |