Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs730882002 | 0.925 | 0.040 | 17 | 7674956 | missense variant | T/C | snv | 6 | |||
rs10248565 | 1.000 | 0.040 | 7 | 18935100 | intron variant | T/G | snv | 0.14 | 3 | ||
rs767505234 | 1.000 | 0.040 | 7 | 55174033 | missense variant | C/T | snv | 1.4E-05 | 3 | ||
rs977818812 | 1.000 | 0.040 | 17 | 39723608 | missense variant | A/T | snv | 3 | |||
rs1057519731 | 0.925 | 0.040 | 15 | 66436816 | missense variant | G/C | snv | 2 | |||
rs1057519785 | 1.000 | 0.040 | 2 | 29222404 | missense variant | A/C | snv | 2 | |||
rs1057519787 | 1.000 | 0.040 | 17 | 39711952 | missense variant | G/A;C | snv | 2 | |||
rs1057519856 | 0.925 | 0.040 | 15 | 66436815 | missense variant | T/A | snv | 2 | |||
rs1131692237 | 1.000 | 0.040 | 17 | 39725161 | missense variant | T/G | snv | 2 | |||
rs1131692238 | 0.925 | 0.040 | 17 | 39509731 | missense variant | G/T | snv | 2 | |||
rs1315148641 | 1.000 | 0.040 | 12 | 7654617 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs1356083197 | 1.000 | 0.040 | 1 | 224434068 | missense variant | C/T | snv | 1.5E-05 | 1.4E-05 | 2 | |
rs1431090090 | 1.000 | 0.040 | 10 | 31520347 | missense variant | C/A | snv | 4.0E-06 | 2 | ||
rs1464381306 | 1.000 | 0.040 | 17 | 64390632 | missense variant | A/T | snv | 1.4E-05 | 2 | ||
rs16970006 | 1.000 | 0.040 | 15 | 78677917 | intron variant | T/C | snv | 8.7E-02 | 2 | ||
rs200298588 | 1.000 | 0.040 | 4 | 94575722 | missense variant | G/A | snv | 2 | |||
rs2004038 | 1.000 | 0.040 | 15 | 78779064 | intron variant | G/A | snv | 0.33 | 2 | ||
rs2608029 | 1.000 | 0.040 | 8 | 128157880 | intron variant | C/G | snv | 0.37 | 2 | ||
rs3885951 | 1.000 | 0.040 | 15 | 78533575 | missense variant | A/G | snv | 7.5E-02 | 6.9E-02 | 2 | |
rs4947492 | 0.925 | 0.040 | 7 | 55120299 | intron variant | G/A | snv | 0.50 | 2 | ||
rs746540053 | 1.000 | 0.040 | 1 | 207911034 | missense variant | C/T | snv | 2 | |||
rs754284524 | 1.000 | 0.040 | 5 | 122074125 | stop gained | -/TACATGCTAGATTCATTTTAACTCAATACTGCCATTCAATTCTAGCAAC | ins | 4.0E-06 | 2 | ||
rs759404153 | 1.000 | 0.040 | 1 | 22910452 | missense variant | T/A;G | snv | 2.8E-05; 4.0E-06 | 2 | ||
rs78442819 | 1.000 | 0.040 | 16 | 10647125 | intron variant | G/C | snv | 0.13 | 2 | ||
rs896171398 | 1.000 | 0.040 | 17 | 39709846 | missense variant | G/A;C | snv | 1.6E-05 | 2 |