Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11099098 | 0.925 | 0.120 | 4 | 80248758 | intergenic variant | G/C;T | snv | 8 | |||
rs1173766 | 5 | 32804422 | intergenic variant | T/C | snv | 0.57 | 5 | ||||
rs1173771 | 5 | 32814922 | regulatory region variant | A/G | snv | 0.65 | 9 | ||||
rs13002573 | 2 | 164058698 | intron variant | A/G | snv | 0.20 | 3 | ||||
rs13082711 | 3 | 27496418 | intergenic variant | T/C | snv | 0.16 | 5 | ||||
rs13149993 | 4 | 80237391 | regulatory region variant | G/A;C | snv | 6 | |||||
rs13209747 | 6 | 126794309 | intron variant | C/G;T | snv | 0.36 | 5 | ||||
rs1327235 | 20 | 10988382 | intron variant | A/G | snv | 0.46 | 7 | ||||
rs1446468 | 2 | 164106976 | intron variant | T/C | snv | 0.40 | 4 | ||||
rs1458038 | 0.925 | 0.120 | 4 | 80243569 | intergenic variant | C/T | snv | 0.23 | 10 | ||
rs16849225 | 2 | 164050310 | intron variant | C/T | snv | 0.19 | 5 | ||||
rs16998073 | 0.925 | 0.120 | 4 | 80263187 | upstream gene variant | A/G;T | snv | 10 | |||
rs17428471 | 7 | 27298248 | intergenic variant | G/T | snv | 9.4E-02 | 3 | ||||
rs17477177 | 1.000 | 0.080 | 7 | 106771412 | upstream gene variant | T/C | snv | 0.17 | 4 | ||
rs2969070 | 7 | 2472910 | downstream gene variant | G/A;C | snv | 3 | |||||
rs35444 | 12 | 115114632 | intergenic variant | A/G | snv | 0.38 | 6 | ||||
rs4842666 | 12 | 89547772 | non coding transcript exon variant | T/C | snv | 0.16 | 3 | ||||
rs6495122 | 1.000 | 0.040 | 15 | 74833304 | downstream gene variant | A/C | snv | 0.44 | 6 | ||
rs12946454 | 0.925 | 0.040 | 17 | 45130754 | intron variant | A/T | snv | 0.21 | 5 | ||
rs2004776 | 1 | 230712956 | intron variant | C/G;T | snv | 5 | |||||
rs2493134 | 1 | 230713613 | intron variant | T/C | snv | 0.57 | 4 | ||||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 | |
rs7129220 | 11 | 10328991 | intron variant | G/A | snv | 0.10 | 5 | ||||
rs604723 | 1.000 | 0.040 | 11 | 100739815 | intron variant | T/C | snv | 0.78 | 9 | ||
rs633185 | 0.925 | 0.080 | 11 | 100722807 | intron variant | G/A;C | snv | 10 |