Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs76064236 | 1.000 | 0.080 | 1 | 226335330 | upstream gene variant | T/G | snv | 2.1E-03 | 1 | ||
rs77138376 | 1.000 | 0.080 | 1 | 78168337 | downstream gene variant | G/A;C | snv | 1 | |||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs2292832 | 0.605 | 0.640 | 2 | 240456086 | non coding transcript exon variant | T/A;C | snv | 0.59 | 46 | ||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 44 | ||
rs5742909 | 0.614 | 0.680 | 2 | 203867624 | upstream gene variant | C/T | snv | 6.7E-02 | 40 | ||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs4553808 | 0.672 | 0.320 | 2 | 203866282 | upstream gene variant | A/G;T | snv | 0.16 | 28 | ||
rs767830104 | 0.752 | 0.280 | 2 | 136115399 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 | 13 | ||
rs1372834938 | 0.763 | 0.280 | 2 | 8812465 | missense variant | G/C | snv | 4.2E-06 | 12 | ||
rs188942711 | 0.763 | 0.200 | 2 | 227253336 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 9 | ||
rs16840252 | 0.776 | 0.480 | 2 | 203866796 | upstream gene variant | C/T | snv | 0.16 | 8 | ||
rs121908525 | 0.790 | 0.160 | 2 | 240875159 | missense variant | T/C | snv | 4.4E-05 | 5.6E-05 | 7 | |
rs452204 | 0.807 | 0.200 | 2 | 113131484 | intron variant | G/A | snv | 0.45 | 7 | ||
rs13538 | 1.000 | 0.080 | 2 | 73641201 | missense variant | A/G | snv | 0.21 | 0.31 | 5 | |
rs7422339 | 1.000 | 0.080 | 2 | 210675783 | missense variant | C/A | snv | 5 | |||
rs121908529 | 0.851 | 0.160 | 2 | 240871433 | missense variant | G/A;C | snv | 5.6E-04 | 4 | ||
rs187355703 | 1.000 | 0.080 | 2 | 176128855 | intron variant | C/G | snv | 1.5E-02 | 1.5E-02 | 4 | |
rs6431731 | 1.000 | 0.080 | 2 | 15722878 | intron variant | C/T | snv | 0.97 | 4 | ||
rs7588550 | 0.851 | 0.160 | 2 | 212304043 | intron variant | G/A | snv | 0.96 | 4 | ||
rs11123169 | 1.000 | 0.080 | 2 | 113209498 | upstream gene variant | C/A;T | snv | 3 | |||
rs11571317 | 0.882 | 0.160 | 2 | 203867285 | upstream gene variant | C/T | snv | 5.2E-02 | 3 | ||
rs3764913 | 1.000 | 0.080 | 2 | 210210185 | non coding transcript exon variant | T/C | snv | 0.30 | 0.27 | 3 | |
rs4972593 | 0.925 | 0.200 | 2 | 173598126 | intergenic variant | T/A | snv | 0.20 | 3 |