Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs439401 | 0.851 | 0.200 | 19 | 44911194 | non coding transcript exon variant | T/C | snv | 0.68 | 8 | ||
rs145579007 | 0.925 | 0.080 | 17 | 63496503 | missense variant | G/A | snv | 1.0E-04 | 1.0E-04 | 2 | |
rs750712925 | 0.925 | 0.080 | 17 | 63477227 | missense variant | G/A;C;T | snv | 3.2E-05 | 2 | ||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1799722 | 0.882 | 0.240 | 14 | 96204802 | 5 prime UTR variant | C/T | snv | 0.41 | 0.39 | 4 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs3792738 | 1.000 | 0.040 | 5 | 76951959 | upstream gene variant | C/A;G | snv | 1 | |||
rs110402 | 0.790 | 0.120 | 17 | 45802681 | intron variant | G/A;C | snv | 12 | |||
rs2228305 | 0.925 | 0.120 | 17 | 82084916 | missense variant | C/T | snv | 4.1E-02 | 4.5E-02 | 3 | |
rs1360780 | 0.708 | 0.320 | 6 | 35639794 | intron variant | T/A;C | snv | 31 | |||
rs5479 | 0.925 | 0.080 | 16 | 67435830 | synonymous variant | C/A;G;T | snv | 5.4E-02; 8.0E-06; 4.0E-06 | 3 | ||
rs56303414 | 0.925 | 0.080 | 16 | 67432532 | intron variant | C/G | snv | 0.55 | 2 | ||
rs1861494 | 0.716 | 0.400 | 12 | 68157629 | intron variant | C/T | snv | 0.75 | 15 | ||
rs2430561 | 0.590 | 0.760 | 12 | 68158742 | intron variant | T/A | snv | 0.36 | 50 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs1143643 | 0.790 | 0.320 | 2 | 112830725 | intron variant | C/T | snv | 0.29 | 10 | ||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs324981 | 0.724 | 0.320 | 7 | 34778501 | missense variant | A/T | snv | 0.44 | 0.47 | 18 | |
rs56149945 | 0.595 | 0.680 | 5 | 143399752 | missense variant | T/A;C | snv | 2.0E-02 | 49 | ||
rs53576 | 0.641 | 0.320 | 3 | 8762685 | intron variant | A/G;T | snv | 42 | |||
rs3087879 | 0.925 | 0.080 | 9 | 4586808 | 3 prime UTR variant | G/C | snv | 0.28 | 2 | ||
rs222747 | 0.827 | 0.240 | 17 | 3589906 | missense variant | C/A;G;T | snv | 0.72; 4.5E-06 | 8 |