Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 | |||||
rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 3 | |||
rs10206899 | 2 | 73673773 | intron variant | T/C;G | snv | 0.21; 3.9E-05 | 2 | ||||
rs10032549 | 4 | 76476862 | intron variant | A/G | snv | 0.43 | 1 | ||||
rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 1 | ||||
rs11078893 | 17 | 39240426 | intron variant | T/C | snv | 0.67 | 1 | ||||
rs12124078 | 1 | 15543404 | intron variant | A/G | snv | 0.32 | 1 | ||||
rs16853722 | 3 | 169432844 | intron variant | T/C | snv | 0.11 | 1 | ||||
rs17536527 | 15 | 45426989 | upstream gene variant | G/A;C | snv | 1 | |||||
rs2068888 | 10 | 93079885 | downstream gene variant | G/A | snv | 0.42 | 1 | ||||
rs2453580 | 17 | 19535008 | non coding transcript exon variant | T/C | snv | 0.37 | 1 | ||||
rs2834317 | 21 | 33984405 | regulatory region variant | G/A | snv | 0.11 | 1 | ||||
rs2842870 | 1 | 156230880 | intron variant | T/A;C | snv | 1 | |||||
rs2928148 | 15 | 41109352 | intron variant | G/A | snv | 0.44 | 1 | ||||
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 1 | ||||
rs4795384 | 17 | 39560518 | intron variant | C/G | snv | 0.68 | 1 | ||||
rs4859682 | 4 | 76489165 | intron variant | C/A | snv | 0.33 | 1 | ||||
rs6440003 | 3 | 141375367 | intron variant | G/A | snv | 0.54 | 1 | ||||
rs6499166 | 16 | 68293014 | intron variant | G/A | snv | 0.79 | 1 | ||||
rs6862195 | 5 | 177395511 | intron variant | G/T | snv | 0.29 | 1 | ||||
rs7624084 | 3 | 141374443 | intron variant | T/C | snv | 0.54 | 1 | ||||
rs9916302 | 17 | 39343696 | intron variant | T/C | snv | 0.35 | 1 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 17 |