Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11677607 | 2 | 100134688 | intron variant | C/T | snv | 0.24 | 1 | ||||
rs73966422 | 2 | 100137627 | non coding transcript exon variant | C/G;T | snv | 1 | |||||
rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
rs400301 | 3 | 10015782 | intron variant | G/A | snv | 6.8E-02 | 1 | ||||
rs57989773 | 1.000 | 0.080 | 6 | 100181202 | downstream gene variant | T/C | snv | 0.23 | 2 | ||
rs13002946 | 2 | 100185497 | intron variant | T/A | snv | 0.25 | 1 | ||||
rs6542924 | 2 | 100276651 | 3 prime UTR variant | C/A;G | snv | 1 | |||||
rs4851287 | 2 | 100299310 | missense variant | A/G | snv | 0.69 | 0.72 | 1 | |||
rs9299338 | 9 | 100345896 | intron variant | A/G;T | snv | 1 | |||||
rs17094222 | 0.925 | 0.080 | 10 | 100635683 | intergenic variant | T/C | snv | 0.17 | 3 | ||
rs2495707 | 10 | 100666192 | downstream gene variant | A/G | snv | 0.21 | 1 | ||||
rs12147845 | 14 | 100678259 | intron variant | C/T | snv | 0.10 | 1 | ||||
rs180963 | 6 | 100679337 | intron variant | T/C | snv | 0.52 | 1 | ||||
rs41310284 | 10 | 100687890 | intergenic variant | C/A;T | snv | 3 | |||||
rs6907240 | 6 | 100705906 | intron variant | T/C;G | snv | 1 | |||||
rs12209887 | 6 | 100708930 | intron variant | G/A | snv | 0.47 | 1 | ||||
rs34277166 | 10 | 100875096 | regulatory region variant | G/A | snv | 0.40 | 1 | ||||
rs1799805 | 7 | 100893176 | missense variant | G/T | snv | 4.0E-02 | 3.2E-02 | 1 | |||
rs10883560 | 10 | 100913950 | intron variant | C/G;T | snv | 1 | |||||
rs3134353 | 8 | 100935225 | intron variant | A/C;G;T | snv | 1 | |||||
rs3134358 | 8 | 100946205 | intron variant | G/T | snv | 0.66 | 1 | ||||
rs7817485 | 8 | 100957300 | upstream gene variant | T/C;G | snv | 0.66 | 1 | ||||
rs7161194 | 14 | 101062668 | upstream gene variant | A/G;T | snv | 2 | |||||
rs7147503 | 14 | 101073047 | intron variant | C/T | snv | 0.32 | 1 | ||||
rs12431682 | 14 | 101073662 | intron variant | C/T | snv | 0.32 | 1 |