Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61871342 | 1.000 | 0.040 | 10 | 100278884 | intron variant | G/A | snv | 0.36 | 2 | ||
rs13107612 | 0.827 | 0.120 | 4 | 101818823 | intron variant | C/T | snv | 0.31 | 5 | ||
rs17266594 | 0.807 | 0.280 | 4 | 101829765 | intron variant | T/C | snv | 0.25 | 0.27 | 7 | |
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 11 | ||
rs3733197 | 0.742 | 0.320 | 4 | 101918130 | missense variant | G/A | snv | 0.31 | 0.30 | 13 | |
rs7637230 | 0.925 | 0.040 | 3 | 101944711 | intron variant | A/G;T | snv | 2 | |||
rs4851529 | 0.827 | 0.120 | 2 | 102030838 | downstream gene variant | G/A | snv | 0.44 | 5 | ||
rs871656 | 0.827 | 0.120 | 2 | 102154822 | intron variant | T/A;C | snv | 5 | |||
rs12987977 | 0.827 | 0.120 | 2 | 102358876 | intron variant | T/G | snv | 0.31 | 5 | ||
rs2075184 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 14 | ||
rs3774937 | 0.776 | 0.280 | 4 | 102513096 | intron variant | T/C | snv | 0.26 | 9 | ||
rs1020760 | 0.925 | 0.040 | 4 | 102593288 | non coding transcript exon variant | C/G | snv | 0.42 | 2 | ||
rs7665090 | 0.807 | 0.280 | 4 | 102630446 | downstream gene variant | A/G | snv | 0.55 | 6 | ||
rs12972990 | 1.000 | 0.040 | 19 | 10295755 | intron variant | T/G | snv | 0.35 | 1 | ||
rs73510898 | 0.925 | 0.120 | 19 | 10305768 | intron variant | G/A;C;T | snv | 2 | |||
rs74956615 | 0.807 | 0.160 | 19 | 10317045 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs34536443 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 25 | |
rs35018800 | 0.790 | 0.160 | 19 | 10354167 | missense variant | G/A | snv | 4.6E-03 | 4.9E-03 | 9 | |
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
rs280519 | 0.752 | 0.320 | 19 | 10362257 | splice region variant | A/C;G | snv | 0.50 | 10 | ||
rs1002212321 | 1.000 | 0.040 | 8 | 103931366 | missense variant | T/C | snv | 1 | |||
rs527418169 | 1.000 | 0.040 | 8 | 104093501 | missense variant | G/A;T | snv | 4.4E-06; 4.4E-06 | 1 | ||
rs11053802 | 1.000 | 0.040 | 12 | 10444608 | intron variant | C/G;T | snv | 1 | |||
rs1051738 | 1.000 | 0.040 | 19 | 10467167 | missense variant | C/A;T | snv | 0.17; 4.8E-05 | 1 | ||
rs62131887 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 14 |