Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1936807 | 6 | 127127104 | intron variant | C/G | snv | 0.55 | 4 | ||||
rs2968478 | 16 | 88792238 | intergenic variant | T/G | snv | 0.61 | 4 | ||||
rs4791641 | 17 | 8257831 | missense variant | C/T | snv | 0.43 | 0.41 | 4 | |||
rs6415788 | 9 | 4118111 | missense variant | G/T | snv | 0.67 | 0.62 | 4 | |||
rs837763 | 16 | 88787321 | upstream gene variant | C/G;T | snv | 4 | |||||
rs10168349 | 2 | 46133768 | intron variant | G/C | snv | 0.36 | 3 | ||||
rs10495928 | 2 | 46126027 | intron variant | A/G | snv | 0.36 | 3 | ||||
rs114948639 | 2 | 46066687 | intron variant | C/T | snv | 7.2E-03 | 3 | ||||
rs115986297 | 6 | 2050557 | intron variant | A/C;G | snv | 3 | |||||
rs11689538 | 2 | 121238062 | intron variant | G/C | snv | 0.11 | 3 | ||||
rs1256061 | 14 | 64236875 | intron variant | G/A;T | snv | 3 | |||||
rs12811512 | 12 | 12893277 | intron variant | C/T | snv | 0.11 | 3 | ||||
rs149804345 | 3 | 56710234 | intergenic variant | AACAAA/-;AACAAAAACAAA;AACAAAAACAAAAACAAA | delins | 3 | |||||
rs17287978 | 6 | 43973400 | intergenic variant | T/C | snv | 3.3E-02 | 3 | ||||
rs17773190 | 2 | 46803224 | intron variant | A/G | snv | 0.32 | 3 | ||||
rs1997595 | 21 | 15205839 | intron variant | A/C;G | snv | 3 | |||||
rs2269188 | 21 | 36700056 | intron variant | G/C | snv | 0.24 | 3 | ||||
rs2732480 | 12 | 48342520 | 3 prime UTR variant | C/A | snv | 0.39 | 3 | ||||
rs35060063 | 3 | 194956076 | intergenic variant | G/A | snv | 0.36 | 3 | ||||
rs35542019 | 21 | 33974555 | non coding transcript exon variant | AA/-;A | delins | 0.57 | 3 | ||||
rs366684 | 1 | 214013919 | intron variant | G/A;C | snv | 3 | |||||
rs3847858 | 12 | 51924594 | downstream gene variant | A/T | snv | 8.9E-02 | 3 | ||||
rs4760682 | 12 | 48118502 | missense variant | C/A | snv | 0.85 | 0.87 | 3 | |||
rs4823308 | 22 | 45604058 | downstream gene variant | T/A | snv | 0.38 | 3 | ||||
rs533281866 | 1 | 231422308 | intron variant | G/A;C | snv | 3 |