Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10181656 | 0.763 | 0.360 | 2 | 191105153 | intron variant | G/C | snv | 0.79 | 1 | ||
rs10865331 | 0.827 | 0.120 | 2 | 62324337 | intergenic variant | A/G | snv | 0.57 | 5 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs114212579 | 1.000 | 0.080 | 6 | 31968280 | non coding transcript exon variant | G/T | snv | 1 | |||
rs114265779 | 1.000 | 0.080 | 6 | 30213844 | upstream gene variant | C/T | snv | 1 | |||
rs114383947 | 1.000 | 0.080 | 6 | 31010940 | intron variant | C/T | snv | 1 | |||
rs114598684 | 1.000 | 0.080 | 6 | 31413173 | intron variant | C/T | snv | 1 | |||
rs114757170 | 1.000 | 0.080 | 6 | 30618254 | intron variant | G/A | snv | 1 | |||
rs115112280 | 1.000 | 0.080 | 6 | 32390772 | non coding transcript exon variant | T/A;G | snv | 1 | |||
rs115145466 | 1.000 | 0.080 | 6 | 32251264 | upstream gene variant | C/A;T | snv | 1 | |||
rs115429782 | 1.000 | 0.080 | 6 | 31297975 | intron variant | T/C | snv | 1 | |||
rs115429849 | 1.000 | 0.080 | 6 | 30416827 | intron variant | G/A | snv | 1 | |||
rs115529844 | 1.000 | 0.080 | 6 | 29850244 | non coding transcript exon variant | C/T | snv | 1 | |||
rs115618145 | 1.000 | 0.080 | 6 | 30102498 | upstream gene variant | C/G | snv | 1 | |||
rs115645848 | 1.000 | 0.080 | 6 | 29622938 | intron variant | C/G;T | snv | 1 | |||
rs115872194 | 1.000 | 0.080 | 6 | 31639897 | intron variant | C/A;T | snv | 1 | |||
rs115928623 | 1.000 | 0.080 | 6 | 29971371 | intron variant | A/T | snv | 1 | |||
rs116199901 | 1.000 | 0.080 | 6 | 30315875 | intron variant | G/C | snv | 1 | |||
rs116340302 | 1.000 | 0.080 | 6 | 31528604 | non coding transcript exon variant | A/T | snv | 1 | |||
rs116805908 | 1.000 | 0.080 | 6 | 31173746 | non coding transcript exon variant | C/T | snv | 1 | |||
rs12044149 | 0.925 | 0.080 | 1 | 67135003 | intron variant | G/C;T | snv | 1 | |||
rs12188300 | 0.807 | 0.120 | 5 | 159402519 | intron variant | A/G;T | snv | 6 | |||
rs12191877 | 0.851 | 0.120 | 6 | 31285148 | intron variant | C/T | snv | 0.12 | 2 | ||
rs12356475 | 1.000 | 0.080 | 10 | 66001962 | intron variant | T/C | snv | 0.15 | 1 | ||
rs13017599 | 0.882 | 0.160 | 2 | 60937196 | non coding transcript exon variant | G/A | snv | 0.25 | 2 |