Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 25 | |
rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 23 | ||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 18 | ||
rs174533 | 0.763 | 0.160 | 11 | 61781553 | intron variant | G/A | snv | 0.37 | 0.29 | 17 | |
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 16 | |||
rs174537 | 0.708 | 0.400 | 11 | 61785208 | non coding transcript exon variant | G/T | snv | 0.28 | 14 | ||
rs174594 | 0.776 | 0.160 | 11 | 61852357 | intron variant | C/A;T | snv | 13 | |||
rs12509595 | 1.000 | 0.080 | 4 | 80261400 | intergenic variant | T/C | snv | 0.23 | 10 | ||
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 10 | ||
rs603424 | 1.000 | 0.080 | 10 | 100315722 | intron variant | G/A | snv | 0.34 | 10 | ||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs174549 | 0.851 | 0.240 | 11 | 61803910 | 5 prime UTR variant | G/A | snv | 0.26 | 8 | ||
rs963837 | 0.925 | 0.120 | 11 | 30727543 | intergenic variant | T/C | snv | 0.35 | 8 | ||
rs9895661 | 0.882 | 0.200 | 17 | 61379228 | non coding transcript exon variant | C/T | snv | 0.69 | 7 | ||
rs3087243 | 0.623 | 0.720 | 2 | 203874196 | downstream gene variant | G/A | snv | 0.37 | 7 | ||
rs174566 | 0.925 | 0.160 | 11 | 61824890 | intron variant | A/G | snv | 0.34 | 7 | ||
rs174583 | 0.807 | 0.320 | 11 | 61842278 | intron variant | C/T | snv | 0.35 | 7 | ||
rs11622435 | 0.827 | 0.120 | 14 | 81151652 | intron variant | G/A | snv | 4.7E-02 | 7 | ||
rs77924615 | 1.000 | 0.080 | 16 | 20381010 | intron variant | G/A | snv | 0.16 | 7 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 6 | |
rs174554 | 1.000 | 0.080 | 11 | 61811991 | intron variant | A/G | snv | 0.40 | 0.28 | 6 | |
rs7740107 | 1.000 | 0.080 | 6 | 130053316 | intron variant | T/A;G | snv | 6 | |||
rs3925584 | 1.000 | 0.080 | 11 | 30738788 | intergenic variant | T/C | snv | 0.35 | 6 |