Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9273363 | 0.851 | 0.280 | 6 | 32658495 | upstream gene variant | C/A | snv | 0.23 | 4 | ||
rs9268831 | 0.851 | 0.280 | 6 | 32459971 | non coding transcript exon variant | C/T | snv | 0.54 | 0.51 | 4 | |
rs539703 | 0.882 | 0.200 | 6 | 32320685 | intron variant | A/C;T | snv | 4 | |||
rs926591 | 0.882 | 0.200 | 6 | 32337913 | intron variant | C/A | snv | 0.33 | 4 | ||
rs4959093 | 0.882 | 0.200 | 6 | 32345320 | intron variant | T/C | snv | 0.33 | 4 | ||
rs574710 | 0.882 | 0.200 | 6 | 32320413 | intron variant | T/C | snv | 0.34 | 4 | ||
rs9368716 | 0.882 | 0.200 | 6 | 32338313 | intron variant | G/A | snv | 0.39 | 4 | ||
rs2859998 | 0.882 | 0.080 | 8 | 58411603 | intron variant | G/A | snv | 0.30 | 4 | ||
rs1086603 | 0.882 | 0.120 | 1 | 147816164 | intergenic variant | G/A | snv | 3.4E-02 | 3 | ||
rs12425451 | 0.882 | 0.080 | 12 | 3055757 | TF binding site variant | C/T | snv | 0.54 | 3 | ||
rs1461347 | 0.882 | 0.120 | 11 | 37191871 | intergenic variant | T/C | snv | 4.5E-02 | 3 | ||
rs16830359 | 1.000 | 0.080 | 1 | 43130713 | intergenic variant | G/A;T | snv | 3 | |||
rs17138435 | 0.882 | 0.120 | 11 | 79481943 | TF binding site variant | A/C;G | snv | 1.6E-02 | 3 | ||
rs17167034 | 0.882 | 0.120 | 7 | 88488811 | intron variant | A/G | snv | 1.4E-02 | 3 | ||
rs17754109 | 0.882 | 0.120 | 9 | 17130158 | upstream gene variant | C/T | snv | 4.7E-02 | 3 | ||
rs2647046 | 0.882 | 0.200 | 6 | 32700559 | TF binding site variant | A/C | snv | 0.64 | 3 | ||
rs3115576 | 0.882 | 0.200 | 6 | 32249073 | intergenic variant | T/A | snv | 0.41 | 3 | ||
rs3130311 | 0.882 | 0.200 | 6 | 32249590 | intergenic variant | A/G;T | snv | 3 | |||
rs3134926 | 0.882 | 0.200 | 6 | 32232370 | intergenic variant | C/A;G | snv | 3 | |||
rs4327572 | 0.882 | 0.120 | 5 | 25972712 | intron variant | C/T | snv | 0.28 | 3 | ||
rs455674 | 0.882 | 0.120 | 6 | 39768626 | regulatory region variant | C/G;T | snv | 3 | |||
rs6023560 | 0.882 | 0.120 | 20 | 54743554 | intergenic variant | A/C;G;T | snv | 0.12 | 3 | ||
rs7756262 | 0.882 | 0.200 | 6 | 32430898 | intergenic variant | T/A | snv | 0.38 | 3 | ||
rs9267954 | 0.882 | 0.200 | 6 | 32245275 | regulatory region variant | A/C;T | snv | 3 | |||
rs9267971 | 0.882 | 0.200 | 6 | 32249408 | intergenic variant | T/C | snv | 0.41 | 3 |