Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7544735 | 1.000 | 0.040 | 1 | 220825571 | intron variant | G/A | snv | 0.22 | 3 | ||
rs10489202 | 0.925 | 0.080 | 1 | 167933841 | intron variant | G/T | snv | 0.20 | 2 | ||
rs11264339 | 1.000 | 0.040 | 1 | 155168172 | downstream gene variant | C/T | snv | 0.56 | 2 | ||
rs11265022 | 1.000 | 0.040 | 1 | 158542829 | downstream gene variant | T/A | snv | 0.21 | 2 | ||
rs12094989 | 1.000 | 0.040 | 1 | 26521895 | upstream gene variant | C/T | snv | 0.29 | 2 | ||
rs16840314 | 1.000 | 0.040 | 1 | 158547563 | synonymous variant | G/A | snv | 0.23 | 0.19 | 2 | |
rs2241107 | 1.000 | 0.040 | 1 | 156212919 | upstream gene variant | T/C;G | snv | 2 | |||
rs2253677 | 1.000 | 0.040 | 1 | 156201505 | intron variant | C/G | snv | 0.42 | 2 | ||
rs2297141 | 0.925 | 0.080 | 1 | 85581241 | non coding transcript exon variant | G/A;C | snv | 2 | |||
rs2785663 | 1.000 | 0.040 | 1 | 157650968 | intergenic variant | T/G | snv | 0.64 | 2 | ||
rs2853641 | 1.000 | 0.040 | 1 | 156211979 | 3 prime UTR variant | A/G | snv | 0.43 | 2 | ||
rs6576776 | 0.925 | 0.080 | 1 | 85584394 | downstream gene variant | C/A;G | snv | 2 | |||
rs6670311 | 1.000 | 0.040 | 1 | 26538994 | intron variant | C/G | snv | 4.4E-02 | 2 | ||
rs863344 | 1.000 | 0.040 | 1 | 158565041 | intron variant | G/A | snv | 0.19 | 2 | ||
rs863345 | 0.925 | 0.080 | 1 | 158565192 | intron variant | C/T | snv | 0.54 | 2 | ||
rs10399681 | 1.000 | 0.040 | 1 | 158555761 | upstream gene variant | G/A | snv | 0.50 | 1 | ||
rs10429895 | 1.000 | 0.040 | 1 | 190689509 | intron variant | C/T | snv | 0.32 | 1 | ||
rs10489573 | 1.000 | 0.040 | 1 | 18358708 | intron variant | C/T | snv | 0.21 | 1 | ||
rs10489676 | 1.000 | 0.040 | 1 | 157650099 | intergenic variant | T/C | snv | 0.24 | 1 | ||
rs10493240 | 1.000 | 0.040 | 1 | 58318478 | intron variant | G/C;T | snv | 1 | |||
rs10493241 | 1.000 | 0.040 | 1 | 58318299 | intron variant | G/A | snv | 0.13 | 1 | ||
rs10493249 | 1.000 | 0.040 | 1 | 58306455 | intron variant | G/T | snv | 0.14 | 1 | ||
rs10493260 | 1.000 | 0.040 | 1 | 59112910 | intron variant | T/C | snv | 0.11 | 1 | ||
rs10494164 | 1.000 | 0.040 | 1 | 114003906 | intron variant | A/G | snv | 6.7E-02 | 1 | ||
rs10494229 | 1.000 | 0.040 | 1 | 119686494 | intron variant | A/G | snv | 0.23 | 1 |