Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1001007 | 0.827 | 0.120 | 3 | 46387167 | intron variant | A/G;T | snv | 5 | |||
rs1002212321 | 1.000 | 0.040 | 8 | 103931366 | missense variant | T/C | snv | 1 | |||
rs10036748 | 0.752 | 0.360 | 5 | 151078585 | intron variant | C/A;T | snv | 11 | |||
rs1004234 | 0.827 | 0.120 | 5 | 132421409 | intron variant | A/G;T | snv | 5 | |||
rs10088247 | 1.000 | 0.040 | 8 | 3826677 | intron variant | C/T | snv | 0.76 | 1 | ||
rs1008953 | 1.000 | 0.040 | 20 | 45352086 | upstream gene variant | T/C | snv | 0.79 | 1 | ||
rs10094579 | 0.807 | 0.280 | 8 | 89837077 | downstream gene variant | C/A | snv | 0.18 | 6 | ||
rs10180391 | 1.000 | 0.040 | 2 | 85699222 | downstream gene variant | C/T | snv | 0.31 | 1 | ||
rs1020760 | 0.925 | 0.040 | 4 | 102593288 | non coding transcript exon variant | C/G | snv | 0.42 | 2 | ||
rs10405308 | 1.000 | 0.040 | 19 | 1312729 | intergenic variant | G/A | snv | 7.9E-02 | 1 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs1043210477 | 0.701 | 0.520 | 3 | 49358250 | missense variant | G/A | snv | 19 | |||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs1047781 | 0.790 | 0.200 | 19 | 48703374 | missense variant | A/T | snv | 3.6E-02 | 1.2E-02 | 11 | |
rs10484554 | 0.807 | 0.200 | 6 | 31306778 | intron variant | C/T | snv | 0.12 | 11 | ||
rs10484879 | 0.827 | 0.160 | 6 | 52187159 | intron variant | G/A;T | snv | 5 | |||
rs10489628 | 1.000 | 0.040 | 1 | 67238424 | intron variant | G/A | snv | 0.43 | 1 | ||
rs10510607 | 0.827 | 0.120 | 3 | 28244770 | intron variant | C/T | snv | 0.15 | 5 | ||
rs10515778 | 1.000 | 0.040 | 5 | 159231004 | intron variant | A/G | snv | 0.13 | 1 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 11 | ||
rs1051738 | 1.000 | 0.040 | 19 | 10467167 | missense variant | C/A;T | snv | 0.17; 4.8E-05 | 1 | ||
rs1056198 | 0.925 | 0.040 | 20 | 49939692 | intron variant | C/T | snv | 0.34 | 2 | ||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs1062470 | 0.925 | 0.040 | 6 | 31116658 | synonymous variant | G/A | snv | 0.37 | 0.41 | 5 | |
rs10743181 | 0.827 | 0.120 | 11 | 2208529 | regulatory region variant | A/G | snv | 0.77 | 5 |