Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80265967 | 0.732 | 0.200 | 21 | 31667290 | missense variant | A/C;T | snv | 1.4E-03 | 1.2E-03 | 16 | |
rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 9 | |||
rs3849943 | 0.827 | 0.080 | 9 | 27543384 | non coding transcript exon variant | C/G;T | snv | 5 | |||
rs2412208 | 0.827 | 0.080 | 1 | 7032722 | intron variant | T/G | snv | 0.33 | 5 | ||
rs139550538 | 0.827 | 0.080 | 10 | 92524312 | intron variant | T/A | snv | 1.9E-02 | 5 | ||
rs34517613 | 0.827 | 0.080 | 17 | 28283226 | intron variant | C/T | snv | 9.1E-02 | 5 | ||
rs616147 | 0.827 | 0.080 | 3 | 39492990 | intron variant | A/G | snv | 0.76 | 5 | ||
rs35714695 | 0.827 | 0.080 | 17 | 28392769 | intron variant | G/A;T | snv | 0.12 | 5 | ||
rs12608932 | 0.827 | 0.080 | 19 | 17641880 | intron variant | A/C | snv | 0.36 | 5 | ||
rs10029851 | 0.851 | 0.080 | 4 | 108706869 | intergenic variant | A/C;T | snv | 4 | |||
rs1559473 | 0.851 | 0.080 | 2 | 222016799 | intergenic variant | T/G | snv | 0.25 | 4 | ||
rs1605070 | 0.851 | 0.080 | 3 | 51882999 | intergenic variant | C/A | snv | 0.60 | 4 | ||
rs16938145 | 0.851 | 0.080 | 9 | 2256092 | intergenic variant | T/C;G | snv | 4 | |||
rs16975050 | 0.851 | 0.080 | 18 | 41607206 | intron variant | T/G | snv | 7.0E-02 | 4 | ||
rs17162257 | 0.851 | 0.080 | 1 | 26602511 | upstream gene variant | T/A;G | snv | 4 | |||
rs2322978 | 0.851 | 0.080 | 11 | 127846245 | intergenic variant | A/G | snv | 0.74 | 4 | ||
rs4424056 | 0.851 | 0.080 | 6 | 91135689 | intergenic variant | T/G | snv | 0.76 | 4 | ||
rs551585 | 0.851 | 0.080 | 1 | 76660688 | intergenic variant | C/A | snv | 8.9E-02 | 4 | ||
rs6137726 | 0.851 | 0.080 | 20 | 22691782 | intron variant | C/A | snv | 0.25 | 4 | ||
rs7148498 | 0.851 | 0.080 | 14 | 95641618 | intron variant | C/T | snv | 0.12 | 4 | ||
rs72911847 | 0.851 | 0.080 | 2 | 193714051 | intergenic variant | A/G | snv | 3.3E-02 | 4 | ||
rs75285952 | 0.851 | 0.080 | 4 | 27902934 | intergenic variant | G/A | snv | 3.3E-02 | 4 | ||
rs7999075 | 0.851 | 0.080 | 13 | 22046068 | intron variant | C/A | snv | 0.88 | 4 | ||
rs9327881 | 0.851 | 0.080 | 5 | 103389394 | intergenic variant | G/A | snv | 0.13 | 4 | ||
rs9329300 | 0.851 | 0.080 | 10 | 2747402 | intergenic variant | A/C;G | snv | 4 |