Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 8 | |
rs2816992 | 0.925 | 0.040 | 1 | 200100088 | intron variant | A/G | snv | 0.39 | 4 | ||
rs545608 | 0.925 | 0.040 | 1 | 177929986 | intron variant | G/C | snv | 0.20 | 4 | ||
rs1392817 | 0.925 | 0.040 | 1 | 66073773 | intron variant | A/G | snv | 0.51 | 3 | ||
rs10436911 | 0.925 | 0.040 | 1 | 189546287 | intergenic variant | A/G | snv | 8.3E-02 | 2 | ||
rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 2 | ||
rs10493390 | 0.925 | 0.040 | 1 | 65846910 | intron variant | A/C | snv | 1.7E-02 | 2 | ||
rs10753165 | 0.925 | 0.040 | 1 | 177602999 | intron variant | T/A;G | snv | 2 | |||
rs10782606 | 0.925 | 0.040 | 1 | 76215537 | intron variant | G/A | snv | 0.67 | 2 | ||
rs10799667 | 0.925 | 0.040 | 1 | 20840000 | intron variant | T/C | snv | 2.7E-02 | 2 | ||
rs1086512 | 0.925 | 0.040 | 1 | 105694496 | upstream gene variant | G/T | snv | 2.0E-02 | 2 | ||
rs1086603 | 0.882 | 0.120 | 1 | 147816164 | intergenic variant | G/A | snv | 3.4E-02 | 2 | ||
rs10907212 | 0.925 | 0.040 | 1 | 5722661 | intergenic variant | G/A | snv | 0.18 | 2 | ||
rs10910445 | 0.925 | 0.040 | 1 | 232421037 | intron variant | T/A;C | snv | 2 | |||
rs10915816 | 0.925 | 0.040 | 1 | 225374683 | splice region variant | C/T | snv | 0.81 | 0.73 | 2 | |
rs10919410 | 0.925 | 0.040 | 1 | 170460651 | non coding transcript exon variant | T/A;G | snv | 2 | |||
rs10920828 | 0.925 | 0.040 | 1 | 190884663 | intron variant | G/A;C;T | snv | 2 | |||
rs11117615 | 0.925 | 0.040 | 1 | 216551790 | intron variant | T/C | snv | 9.9E-03 | 2 | ||
rs11119283 | 0.925 | 0.040 | 1 | 209467518 | intergenic variant | T/C | snv | 0.36 | 2 | ||
rs11184769 | 0.925 | 0.040 | 1 | 106136142 | intergenic variant | A/G | snv | 5.6E-02 | 2 | ||
rs11207881 | 0.925 | 0.040 | 1 | 61973715 | intron variant | T/C | snv | 3.9E-02 | 2 | ||
rs11240095 | 0.925 | 0.040 | 1 | 147032530 | intron variant | T/A | snv | 0.27 | 2 | ||
rs11264728 | 0.925 | 0.040 | 1 | 157431916 | regulatory region variant | A/G | snv | 0.30 | 2 | ||
rs1175646 | 0.925 | 0.040 | 1 | 112465599 | upstream gene variant | G/A;T | snv | 2 | |||
rs11801558 | 0.925 | 0.040 | 1 | 158369116 | intergenic variant | C/T | snv | 0.18 | 2 |