Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10172053 | 2 | 210779923 | intergenic variant | T/C;G | snv | 2 | |||||
rs1657863 | 2 | 210995002 | intergenic variant | T/G | snv | 0.52 | 2 | ||||
rs4310999 | 2 | 210885574 | intergenic variant | G/A | snv | 0.21 | 2 | ||||
rs4673546 | 2 | 210700968 | intergenic variant | C/T | snv | 0.15 | 2 | ||||
rs4947534 | 7 | 56011401 | 3 prime UTR variant | T/A;C | snv | 2 | |||||
rs651797 | 2 | 210992001 | intergenic variant | G/A | snv | 0.61 | 2 | ||||
rs8059153 | 16 | 81112070 | non coding transcript exon variant | T/C | snv | 0.90 | 2 | ||||
rs12613336 | 2 | 210704675 | regulatory region variant | T/C | snv | 0.19 | 6 | ||||
rs715 | 1.000 | 0.040 | 2 | 210678331 | 3 prime UTR variant | T/C | snv | 0.28 | 13 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 |