Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs115145466 | 1.000 | 0.080 | 6 | 32251264 | upstream gene variant | C/A;T | snv | 1 | |||
rs2621322 | 1.000 | 0.080 | 6 | 32820935 | intron variant | T/G | snv | 0.20 | 1 | ||
rs28780111 | 1.000 | 0.080 | 6 | 30752534 | intron variant | C/G;T | snv | 1 | |||
rs4085613 | 0.827 | 0.160 | 1 | 152577542 | downstream gene variant | T/G | snv | 0.59 | 1 | ||
rs4112788 | 0.851 | 0.120 | 1 | 152578800 | downstream gene variant | A/G;T | snv | 1 | |||
rs115872194 | 1.000 | 0.080 | 6 | 31639897 | intron variant | C/A;T | snv | 1 | |||
rs12044149 | 0.925 | 0.080 | 1 | 67135003 | intron variant | G/C;T | snv | 1 | |||
rs763361 | 0.689 | 0.520 | 18 | 69864406 | missense variant | T/A;C | snv | 4.0E-06; 0.52 | 1 | ||
rs12356475 | 1.000 | 0.080 | 10 | 66001962 | intron variant | T/C | snv | 0.15 | 1 | ||
rs149997688 | 1.000 | 0.080 | 6 | 30893833 | intron variant | G/A | snv | 1 | |||
rs30187 | 0.732 | 0.360 | 5 | 96788627 | missense variant | T/A;C | snv | 0.62 | 1 | ||
rs27044 | 0.827 | 0.240 | 5 | 96783148 | missense variant | G/C | snv | 0.69 | 0.71 | 1 | |
rs115645848 | 1.000 | 0.080 | 6 | 29622938 | intron variant | C/G;T | snv | 1 | |||
rs116199901 | 1.000 | 0.080 | 6 | 30315875 | intron variant | G/C | snv | 1 | |||
rs115112280 | 1.000 | 0.080 | 6 | 32390772 | non coding transcript exon variant | T/A;G | snv | 1 | |||
rs115928623 | 1.000 | 0.080 | 6 | 29971371 | intron variant | A/T | snv | 1 | |||
rs115429782 | 1.000 | 0.080 | 6 | 31297975 | intron variant | T/C | snv | 1 | |||
rs13191343 | 1.000 | 0.080 | 6 | 31273332 | intron variant | C/G;T | snv | 0.13 | 1 | ||
rs9378127 | 1.000 | 0.080 | 6 | 32954682 | intron variant | G/A | snv | 0.11 | 1 | ||
rs28724231 | 1.000 | 0.080 | 6 | 32659314 | upstream gene variant | A/G | snv | 2.9E-02 | 1 | ||
rs1610601 | 1.000 | 0.080 | 6 | 29732406 | intron variant | C/A;T | snv | 0.20 | 1 | ||
rs763780 | 0.531 | 0.720 | 6 | 52236941 | missense variant | T/C | snv | 6.7E-02 | 6.6E-02 | 1 | |
rs4655683 | 1.000 | 0.080 | 1 | 67145930 | intron variant | G/A | snv | 0.37 | 1 | ||
rs145699582 | 1.000 | 0.080 | 9 | 5169600 | intron variant | C/T | snv | 2.5E-03 | 1 | ||
rs115529844 | 1.000 | 0.080 | 6 | 29850244 | non coding transcript exon variant | C/T | snv | 1 |