Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35225200 | 1.000 | 0.040 | 4 | 102225731 | intergenic variant | A/C | snv | 5.4E-02 | 5 | ||
rs4130548 | 1.000 | 0.040 | 1 | 77998184 | intron variant | T/C | snv | 0.25 | 5 | ||
rs12764899 | 1.000 | 0.040 | 10 | 102875346 | intron variant | G/A | snv | 0.21 | 4 | ||
rs4129585 | 1.000 | 0.040 | 8 | 142231572 | intron variant | A/C | snv | 0.68 | 4 | ||
rs6704768 | 1.000 | 0.040 | 2 | 232727791 | intron variant | G/A | snv | 0.54 | 4 | ||
rs6855246 | 1.000 | 0.040 | 4 | 102191313 | intergenic variant | A/G | snv | 0.14 | 4 | ||
rs10752262 | 1.000 | 0.040 | 10 | 12353101 | intron variant | C/T | snv | 0.39 | 3 | ||
rs11210892 | 1.000 | 0.040 | 1 | 43634413 | intergenic variant | G/A | snv | 0.51 | 3 | ||
rs11740474 | 1.000 | 0.040 | 5 | 154301187 | intron variant | A/T | snv | 0.37 | 3 | ||
rs11765189 | 1.000 | 0.040 | 7 | 157743285 | intron variant | A/G | snv | 0.25 | 3 | ||
rs12561919 | 1.000 | 0.040 | 1 | 11779866 | missense variant | C/T | snv | 0.13 | 0.13 | 3 | |
rs12602286 | 1.000 | 0.040 | 17 | 19333641 | intron variant | G/T | snv | 0.79 | 3 | ||
rs12704290 | 1.000 | 0.040 | 7 | 86798310 | intron variant | G/A | snv | 8.9E-02 | 3 | ||
rs12826178 | 1.000 | 0.040 | 12 | 57228588 | upstream gene variant | G/T | snv | 5.3E-02 | 3 | ||
rs133047 | 1.000 | 0.040 | 22 | 40631815 | intron variant | T/C | snv | 0.93 | 3 | ||
rs1408579 | 1.000 | 0.040 | 10 | 100152437 | intron variant | C/T | snv | 0.32 | 3 | ||
rs169738 | 1.000 | 0.040 | 6 | 33569769 | intron variant | A/G;T | snv | 3 | |||
rs2535627 | 1.000 | 0.040 | 3 | 52811089 | downstream gene variant | T/A;C;G | snv | 3 | |||
rs28437878 | 1.000 | 0.040 | 15 | 78515530 | intron variant | C/G;T | snv | 3 | |||
rs28600726 | 1.000 | 0.040 | 4 | 158730723 | intergenic variant | G/A | snv | 0.53 | 3 | ||
rs28669908 | 1.000 | 0.040 | 15 | 78617925 | intron variant | C/A | snv | 0.18 | 3 | ||
rs28681284 | 1.000 | 0.040 | 15 | 78616223 | intron variant | C/T | snv | 0.19 | 3 | ||
rs3617 | 1.000 | 0.040 | 3 | 52799789 | missense variant | C/A | snv | 0.48 | 0.54 | 3 | |
rs3747631 | 1.000 | 0.040 | 1 | 204618441 | missense variant | G/A;C | snv | 4.0E-06; 0.20 | 3 | ||
rs3814883 | 1.000 | 0.040 | 16 | 29983601 | synonymous variant | C/T | snv | 0.44 | 0.37 | 3 |