Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2799573 | 0.851 | 0.040 | 10 | 18312999 | intron variant | T/C | snv | 0.20 | 5 | ||
rs3132581 | 0.851 | 0.040 | 6 | 30945681 | intron variant | G/A | snv | 9.3E-02 | 5 | ||
rs3924999 | 0.851 | 0.040 | 8 | 32595840 | missense variant | G/A | snv | 0.40 | 0.31 | 5 | |
rs548181 | 0.851 | 0.040 | 11 | 125591814 | 5 prime UTR variant | A/G | snv | 0.83 | 5 | ||
rs6465084 | 0.851 | 0.040 | 7 | 86774159 | intron variant | A/G | snv | 0.26 | 5 | ||
rs6484218 | 0.882 | 0.040 | 11 | 10369034 | intron variant | G/A | snv | 0.21 | 5 | ||
rs6694545 | 0.851 | 0.040 | 1 | 29964421 | intergenic variant | A/G | snv | 0.58 | 5 | ||
rs7004633 | 0.851 | 0.040 | 8 | 88748082 | intron variant | A/G | snv | 0.28 | 5 | ||
rs778294 | 0.851 | 0.040 | 13 | 105489886 | synonymous variant | C/A;T | snv | 0.27; 4.0E-06 | 0.26 | 5 | |
rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 5 | ||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 5 | |||
rs945032 | 0.882 | 0.040 | 14 | 96204324 | upstream gene variant | T/C | snv | 0.78 | 5 | ||
rs9951150 | 0.851 | 0.040 | 18 | 55153893 | intergenic variant | A/G;T | snv | 5 | |||
rs10042486 | 0.882 | 0.040 | 5 | 63965502 | intron variant | C/T | snv | 0.58 | 4 | ||
rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
rs1042779 | 0.882 | 0.040 | 3 | 52786995 | missense variant | A/G | snv | 0.40 | 0.42 | 4 | |
rs10447760 | 0.851 | 0.040 | 7 | 114083210 | upstream gene variant | C/T | snv | 0.17 | 4 | ||
rs10458787 | 1.000 | 0.040 | 10 | 4613373 | intergenic variant | A/C;G | snv | 4 | |||
rs10494251 | 0.851 | 0.040 | 1 | 147552120 | intron variant | C/T | snv | 5.8E-02 | 4 | ||
rs10835210 | 0.882 | 0.040 | 11 | 27674363 | intron variant | C/A;G | snv | 4 | |||
rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
rs11004733 | 0.882 | 0.040 | 10 | 55089584 | intron variant | C/T | snv | 2.9E-02 | 4 | ||
rs11682175 | 0.925 | 0.040 | 2 | 57760458 | intron variant | T/C | snv | 0.38 | 4 | ||
rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
rs12476147 | 0.851 | 0.040 | 2 | 184936178 | missense variant | A/T | snv | 0.66 | 0.59 | 4 |