Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10494326 | 1 | 159679910 | intergenic variant | C/T | snv | 5.3E-02 | 1 | ||||
rs10521222 | 16 | 51124799 | intergenic variant | C/T | snv | 3.2E-02 | 1 | ||||
rs11108056 | 12 | 95461609 | regulatory region variant | C/G;T | snv | 1 | |||||
rs111269058 | 7 | 73561372 | upstream gene variant | C/T | snv | 9.8E-02 | 1 | ||||
rs1119582 | 5 | 125907327 | intron variant | T/C | snv | 1 | |||||
rs11265260 | 1.000 | 0.080 | 1 | 159730249 | intergenic variant | A/G | snv | 6.8E-02 | 1 | ||
rs11265263 | 1 | 159740727 | intergenic variant | C/A;T | snv | 1 | |||||
rs12023742 | 1 | 19965513 | intergenic variant | C/A;G | snv | 1 | |||||
rs12029262 | 1 | 159709406 | upstream gene variant | G/C | snv | 8.5E-02 | 1 | ||||
rs12037222 | 1 | 39599289 | regulatory region variant | G/A | snv | 0.16 | 1 | ||||
rs12093699 | 1 | 159678198 | intergenic variant | G/A;C | snv | 0.31 | 1 | ||||
rs12408941 | 1 | 19958994 | intergenic variant | G/A | snv | 9.7E-02 | 1 | ||||
rs12568139 | 1 | 19985183 | upstream gene variant | A/G | snv | 6.0E-02 | 1 | ||||
rs12722987 | 1 | 20128727 | intergenic variant | C/A | snv | 0.17 | 1 | ||||
rs12749227 | 1 | 159689319 | intergenic variant | C/T | snv | 0.25 | 1 | ||||
rs12753193 | 1 | 65703996 | non coding transcript exon variant | G/A | snv | 0.58 | 1 | ||||
rs12960928 | 1.000 | 0.080 | 18 | 60230570 | intergenic variant | T/C | snv | 0.21 | 1 | ||
rs12995480 | 2 | 629881 | intergenic variant | T/C | snv | 0.85 | 1 | ||||
rs13375019 | 1 | 65657453 | intergenic variant | G/C;T | snv | 1 | |||||
rs13375942 | 1 | 19965885 | regulatory region variant | T/A;C;G | snv | 1 | |||||
rs13409371 | 2 | 113080568 | downstream gene variant | G/A;C;T | snv | 1 | |||||
rs1341665 | 1.000 | 0.080 | 1 | 159721769 | intergenic variant | G/A | snv | 0.32 | 1 | ||
rs1408282 | 6 | 93142534 | intergenic variant | G/A | snv | 9.6E-02 | 1 | ||||
rs149520992 | 1 | 159697727 | intergenic variant | C/T | snv | 3.8E-03 | 1 | ||||
rs151233628 | 17 | 6258465 | regulatory region variant | C/G;T | snv | 1 |