Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9461219 | 0.882 | 0.160 | 6 | 25836699 | intron variant | C/G;T | snv | 3 | |||
rs9556958 | 1.000 | 0.040 | 13 | 98447792 | 3 prime UTR variant | C/G;T | snv | 3 | |||
rs9636107 | 1.000 | 0.040 | 18 | 55532886 | intron variant | A/G;T | snv | 3 | |||
rs9841504 | 0.827 | 0.120 | 3 | 114643917 | intron variant | C/G;T | snv | 3 | |||
rs10061788 | 1.000 | 0.040 | 5 | 88638889 | intron variant | G/A;T | snv | 2 | |||
rs1024582 | 1.000 | 0.040 | 12 | 2293080 | intron variant | A/G;T | snv | 2 | |||
rs10520163 | 1.000 | 0.040 | 4 | 169705401 | intron variant | T/A;C | snv | 2 | |||
rs10757417 | 1.000 | 0.040 | 9 | 23347855 | intron variant | G/A;T | snv | 2 | |||
rs1076884 | 1.000 | 0.040 | 16 | 13653946 | intergenic variant | C/G;T | snv | 2 | |||
rs10961430 | 1.000 | 0.040 | 9 | 14224064 | intron variant | G/C;T | snv | 2 | |||
rs11130 | 1.000 | 0.040 | 16 | 15724453 | 3 prime UTR variant | G/A;C | snv | 0.56; 4.0E-06 | 2 | ||
rs111312615 | 1.000 | 0.040 | 6 | 29955302 | upstream gene variant | T/G | snv | 2 | |||
rs11166628 | 1.000 | 0.040 | 8 | 136066082 | intron variant | G/A;C | snv | 2 | |||
rs111977918 | 1.000 | 0.040 | 6 | 31268274 | downstream gene variant | G/A;C | snv | 2 | |||
rs112209031 | 1.000 | 0.040 | 6 | 32524630 | intron variant | T/C;G | snv | 2 | |||
rs1131275 | 1.000 | 0.040 | 6 | 31356183 | missense variant | G/A;C | snv | 0.68 | 2 | ||
rs113205291 | 1.000 | 0.040 | 6 | 29894844 | upstream gene variant | A/G;T | snv | 2 | |||
rs113397282 | 1.000 | 0.040 | 6 | 32520273 | intron variant | T/C;G | snv | 2 | |||
rs114041423 | 1.000 | 0.040 | 6 | 29639270 | upstream gene variant | G/A | snv | 2 | |||
rs114086406 | 1.000 | 0.040 | 6 | 32374760 | intron variant | G/A | snv | 2 | |||
rs114115252 | 1.000 | 0.040 | 6 | 30931418 | 3 prime UTR variant | G/A;C;T | snv | 2 | |||
rs114142645 | 1.000 | 0.040 | 6 | 31245806 | regulatory region variant | T/C | snv | 2 | |||
rs114204022 | 1.000 | 0.040 | 6 | 29972902 | upstream gene variant | G/A | snv | 2 | |||
rs114274203 | 1.000 | 0.040 | 6 | 31300843 | intron variant | C/T | snv | 2 | |||
rs114276265 | 1.000 | 0.040 | 6 | 31219298 | upstream gene variant | C/T | snv | 2 |