Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs537765533 | 0.882 | 0.080 | 2 | 113132839 | missense variant | G/C | snv | 2.0E-05 | 3 | ||
rs539179964 | 0.882 | 0.080 | 8 | 104248720 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 3 | |
rs55791371 | 0.925 | 0.080 | 19 | 11077477 | intron variant | A/C | snv | 0.11 | 3 | ||
rs5629 | 0.925 | 0.080 | 20 | 49513169 | stop gained | G/A;T | snv | 4.0E-06; 0.25 | 3 | ||
rs5940 | 0.882 | 0.080 | 2 | 187466977 | missense variant | C/T | snv | 1.3E-02 | 1.4E-02 | 3 | |
rs61688134 | 0.882 | 0.080 | 12 | 21864476 | missense variant | C/T | snv | 7.4E-03 | 7.5E-03 | 3 | |
rs7213516 | 0.882 | 0.080 | 17 | 63474189 | upstream gene variant | G/A | snv | 5.7E-02 | 3 | ||
rs749903604 | 0.882 | 0.080 | 2 | 21042450 | missense variant | G/A | snv | 8.0E-06 | 3 | ||
rs761646500 | 0.925 | 0.080 | 6 | 169237763 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs779647096 | 0.882 | 0.080 | 6 | 160718313 | synonymous variant | T/C | snv | 1.2E-05 | 7.0E-06 | 3 | |
rs7913948 | 1.000 | 0.080 | 10 | 45373441 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
rs9974610 | 1.000 | 0.080 | 21 | 31646056 | intergenic variant | A/G | snv | 0.13 | 3 | ||
rs1144507 | 0.925 | 0.080 | 11 | 123729767 | missense variant | A/C;G;T | snv | 0.68 | 2 | ||
rs11748327 | 1.000 | 0.080 | 5 | 4029676 | downstream gene variant | C/T | snv | 0.21 | 2 | ||
rs1213545562 | 1.000 | 0.080 | 11 | 2166984 | synonymous variant | G/A | snv | 9.6E-06 | 2 | ||
rs12487736 | 1.000 | 0.080 | 3 | 47418189 | missense variant | C/T | snv | 0.54 | 0.47 | 2 | |
rs12541758 | 0.925 | 0.080 | 8 | 72230147 | non coding transcript exon variant | C/T | snv | 0.34 | 2 | ||
rs1277204441 | 0.925 | 0.080 | 17 | 63479775 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs1380959039 | 1.000 | 0.080 | 10 | 77086524 | synonymous variant | A/G | snv | 4.0E-06 | 2 | ||
rs1384915680 | 1.000 | 0.080 | 11 | 2166903 | synonymous variant | G/A | snv | 4.3E-06 | 2 | ||
rs1395479 | 1.000 | 0.080 | 4 | 177397037 | intergenic variant | C/A;T | snv | 2 | |||
rs16880442 | 0.925 | 0.080 | 5 | 52889863 | non coding transcript exon variant | G/A;T | snv | 2 | |||
rs16964543 | 1.000 | 0.080 | 19 | 30694303 | intron variant | T/C | snv | 0.32 | 2 | ||
rs1722842 | 0.925 | 0.080 | 15 | 23785809 | intron variant | T/C | snv | 0.16 | 2 | ||
rs180803 | 0.925 | 0.080 | 22 | 24262890 | intron variant | G/A;T | snv | 2 |