Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10011838 | 1.000 | 0.080 | 4 | 152599127 | intergenic variant | G/A | snv | 0.42 | 3 | ||
rs10034465 | 1.000 | 0.080 | 4 | 34193882 | intron variant | G/A | snv | 9.1E-02 | 2 | ||
rs1004467 | 0.790 | 0.280 | 10 | 102834750 | non coding transcript exon variant | A/G | snv | 0.15 | 0.14 | 5 | |
rs10077431 | 1.000 | 0.080 | 5 | 113591989 | splice region variant | C/A | snv | 0.15 | 0.16 | 1 | |
rs10087241 | 1.000 | 0.080 | 8 | 31006206 | intron variant | G/A | snv | 0.56 | 1 | ||
rs1009358 | 1.000 | 0.080 | 2 | 65049318 | intron variant | T/C | snv | 0.40 | 2 | ||
rs10100265 | 1.000 | 0.080 | 8 | 10775649 | intron variant | A/C | snv | 0.60 | 1 | ||
rs10114341 | 1.000 | 0.080 | 9 | 94156900 | non coding transcript exon variant | T/C | snv | 0.42 | 1 | ||
rs10146997 | 0.827 | 0.240 | 14 | 79478819 | intron variant | A/G | snv | 0.25 | 2 | ||
rs10169613 | 1.000 | 0.080 | 2 | 111177400 | intron variant | C/T | snv | 0.42 | 1 | ||
rs1017568 | 1.000 | 0.080 | 9 | 3948365 | intron variant | T/C;G | snv | 1 | |||
rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 1 | ||
rs10184004 | 1.000 | 0.080 | 2 | 164651879 | downstream gene variant | C/T | snv | 0.48 | 5 | ||
rs10190052 | 1.000 | 0.080 | 2 | 646674 | intergenic variant | T/C | snv | 0.82 | 1 | ||
rs10195252 | 0.925 | 0.080 | 2 | 164656581 | intron variant | T/C | snv | 0.48 | 6 | ||
rs10203174 | 1.000 | 0.080 | 2 | 43462891 | intron variant | C/T | snv | 0.17 | 1 | ||
rs1020731 | 1.000 | 0.080 | 2 | 160287544 | intron variant | G/A | snv | 0.69 | 1 | ||
rs10224002 | 0.925 | 0.080 | 7 | 151717955 | intron variant | A/G | snv | 0.31 | 8 | ||
rs10228456 | 1.000 | 0.080 | 7 | 15024301 | intergenic variant | C/T | snv | 0.54 | 1 | ||
rs10229583 | 1.000 | 0.080 | 7 | 127606849 | downstream gene variant | G/A | snv | 0.23 | 1 | ||
rs10231021 | 1.000 | 0.080 | 7 | 15020804 | intergenic variant | T/A;G | snv | 1 | |||
rs10244051 | 1.000 | 0.080 | 7 | 15024208 | intergenic variant | T/A;G | snv | 2 | |||
rs10260148 | 1.000 | 0.080 | 7 | 130746210 | intergenic variant | C/T | snv | 0.27 | 2 | ||
rs10261386 | 1.000 | 0.080 | 7 | 121071801 | intron variant | C/T | snv | 0.38 | 1 | ||
rs10278 | 1.000 | 0.080 | 17 | 48862296 | missense variant | C/A;G | snv | 4.0E-05; 0.31 | 1 |