Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10042590 | 5 | 88477501 | intron variant | G/A | snv | 5.8E-02 | 1 | ||||
rs10059884 | 5 | 32832368 | regulatory region variant | C/A;T | snv | 5 | |||||
rs1008805 | 0.851 | 0.160 | 15 | 51257402 | intron variant | G/A | snv | 0.64 | 7 | ||
rs1009358 | 1.000 | 0.080 | 2 | 65049318 | intron variant | T/C | snv | 0.40 | 2 | ||
rs10107066 | 8 | 26542619 | intron variant | G/C | snv | 0.29 | 1 | ||||
rs10116277 | 0.827 | 0.160 | 9 | 22081398 | intron variant | G/T | snv | 0.62 | 8 | ||
rs1022113606 | 0.732 | 0.280 | 4 | 24800161 | missense variant | G/C | snv | 1.6E-04 | 2.1E-05 | 17 | |
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 12 | ||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 9 | ||
rs1030431 | 8 | 58399138 | intergenic variant | A/G;T | snv | 3 | |||||
rs10306135 | 9 | 122375416 | 5 prime UTR variant | A/T | snv | 0.14 | 1 | ||||
rs10409243 | 19 | 10222312 | 3 prime UTR variant | C/A;G;T | snv | 6 | |||||
rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 25 | |
rs1042034 | 0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 | 15 | |
rs1042309696 | 17 | 63487006 | synonymous variant | T/C | snv | 2 | |||||
rs1042580 | 20 | 23046984 | 3 prime UTR variant | T/C | snv | 0.33 | 2 | ||||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs1044250 | 0.807 | 0.240 | 19 | 8371280 | missense variant | C/T | snv | 0.30 | 0.29 | 12 | |
rs1044486 | 17 | 78796097 | 3 prime UTR variant | G/A | snv | 0.41 | 1 | ||||
rs1044498 | 0.752 | 0.360 | 6 | 131851228 | missense variant | A/C;G | snv | 0.19 | 15 | ||
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 33 | ||
rs1047964 | 11 | 117286177 | 3 prime UTR variant | G/A;C;T | snv | 3 | |||||
rs1048070 | 9 | 14735055 | 3 prime UTR variant | T/C | snv | 0.46 | 1 | ||||
rs10500326 | 16 | 4868325 | intron variant | G/T | snv | 0.21 | 1 |