Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10830956 | 1.000 | 0.040 | 11 | 92947847 | intergenic variant | C/T | snv | 0.33 | 1 | ||
rs12545984 | 1.000 | 0.040 | 8 | 19989748 | intergenic variant | C/T | snv | 0.16 | 1 | ||
rs1441756 | 1.000 | 0.040 | 8 | 20010875 | intergenic variant | A/C;G;T | snv | 1 | |||
rs1522813 | 1.000 | 0.040 | 2 | 226080466 | regulatory region variant | G/A | snv | 0.29 | 1 | ||
rs180088 | 1.000 | 0.040 | 17 | 69951455 | intergenic variant | T/A;C | snv | 0.71 | 1 | ||
rs180344 | 1.000 | 0.040 | 11 | 116742468 | regulatory region variant | T/C | snv | 0.34 | 1 | ||
rs1837842 | 1.000 | 0.040 | 8 | 20010779 | intergenic variant | T/C | snv | 0.23 | 1 | ||
rs376021 | 1.000 | 0.040 | 1 | 161555218 | intron variant | T/C | snv | 1.5E-04 | 1 | ||
rs4244457 | 1.000 | 0.040 | 8 | 20041535 | intergenic variant | C/G;T | snv | 1 | |||
rs4442164 | 1.000 | 0.040 | 8 | 20034670 | regulatory region variant | A/G | snv | 0.28 | 1 | ||
rs4449813 | 1.000 | 0.040 | 8 | 20045809 | intergenic variant | G/A | snv | 0.34 | 1 | ||
rs6995374 | 1.000 | 0.040 | 8 | 10468602 | intergenic variant | C/G | snv | 0.22 | 1 | ||
rs916829 | 1.000 | 0.040 | 11 | 17418926 | intron variant | A/G;T | snv | 1 | |||
rs4766587 | 1.000 | 0.040 | 12 | 109247525 | intron variant | G/A | snv | 0.23 | 1 | ||
rs6606697 | 1.000 | 0.040 | 12 | 109173915 | intron variant | A/G | snv | 0.48 | 1 | ||
rs1324805 | 1.000 | 0.040 | X | 109719433 | intron variant | A/G | snv | 0.45 | 1 | ||
rs1133607 | 1.000 | 0.040 | 16 | 20483086 | missense variant | C/G;T | snv | 4.0E-06; 0.13 | 1 | ||
rs13010956 | 1.000 | 0.040 | 2 | 157556030 | intron variant | T/C | snv | 0.39 | 1 | ||
rs1259867035 | 1.000 | 0.040 | 3 | 186854387 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
rs746639990 | 1.000 | 0.040 | 3 | 186854598 | missense variant | A/G | snv | 2.1E-04 | 7.0E-06 | 1 | |
rs10920533 | 1.000 | 0.040 | 1 | 202956690 | intron variant | G/A | snv | 0.22 | 1 | ||
rs17055869 | 1.000 | 0.040 | 8 | 26740131 | intergenic variant | C/A;T | snv | 1 | |||
rs775276843 | 1.000 | 0.040 | 1 | 230710676 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs11631342 | 1.000 | 0.040 | 15 | 58432184 | non coding transcript exon variant | A/G | snv | 5.6E-02 | 1 | ||
rs6511435 | 1.000 | 0.040 | 19 | 10103816 | upstream gene variant | T/A;C;G | snv | 1 |