Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10192369 | 2 | 160524377 | intergenic variant | G/A | snv | 0.45 | 2 | ||||
rs1043595 | 7 | 128769958 | 3 prime UTR variant | G/A | snv | 0.19 | 2 | ||||
rs1046953 | 3 | 50159664 | synonymous variant | C/T | snv | 0.41 | 0.39 | 2 | |||
rs10514301 | 5 | 88643836 | intron variant | C/T | snv | 0.16 | 2 | ||||
rs10514303 | 5 | 88749212 | intron variant | C/A;G | snv | 6.1E-02 | 2 | ||||
rs10783018 | 1 | 95782279 | non coding transcript exon variant | G/A | snv | 0.74 | 2 | ||||
rs10872224 | 6 | 97987249 | intron variant | G/T | snv | 0.67 | 2 | ||||
rs10922907 | 1 | 90727492 | downstream gene variant | A/G;T | snv | 2 | |||||
rs10949662 | 7 | 157741413 | intron variant | C/A;T | snv | 2 | |||||
rs1106761 | 8 | 141609134 | intron variant | G/A | snv | 0.28 | 2 | ||||
rs11076962 | 16 | 5761366 | intron variant | T/C | snv | 0.25 | 2 | ||||
rs11079849 | 17 | 49013423 | intron variant | C/T | snv | 0.28 | 2 | ||||
rs1108842 | 3 | 52686064 | 5 prime UTR variant | A/C;G;T | snv | 0.49; 4.0E-06 | 2 | ||||
rs11142387 | 9 | 70383416 | downstream gene variant | A/C | snv | 0.49 | 2 | ||||
rs11209943 | 1 | 72284817 | intron variant | A/G | snv | 0.53 | 2 | ||||
rs1144 | 7 | 105115908 | intron variant | T/C | snv | 0.31 | 2 | ||||
rs11588857 | 1 | 204617919 | missense variant | G/A;T | snv | 0.20; 8.0E-06 | 2 | ||||
rs11605348 | 11 | 47584931 | upstream gene variant | G/A | snv | 0.28 | 2 | ||||
rs11665567 | 18 | 79803334 | intron variant | G/A | snv | 0.18 | 2 | ||||
rs11793831 | 9 | 23362313 | intron variant | G/A;T | snv | 2 | |||||
rs118134876 | 7 | 11460745 | missense variant | C/A;T | snv | 4.0E-02 | 2 | ||||
rs12446550 | 16 | 28532060 | downstream gene variant | G/A | snv | 0.36 | 2 | ||||
rs12761761 | 10 | 131961871 | downstream gene variant | C/T | snv | 0.21 | 2 | ||||
rs12914495 | 15 | 65687454 | intron variant | A/G;T | snv | 2 | |||||
rs13064915 | 3 | 137402401 | intergenic variant | T/C | snv | 0.42 | 2 |