Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs149454410 | 0.925 | 0.120 | 4 | 9942000 | missense variant | C/G;T | snv | 4.0E-05; 3.2E-04 | 5 | ||
rs143193096 | 15 | 98916098 | missense variant | G/A;C | snv | 8.4E-05; 4.0E-06 | 3 | ||||
rs75248620 | 11 | 9887580 | intron variant | G/A | snv | 5.5E-02 | 1 | ||||
rs4966025 | 15 | 98766313 | intron variant | G/A | snv | 0.60 | 1 | ||||
rs2137683 | 0.925 | 0.120 | 15 | 98746409 | intron variant | C/G | snv | 0.53 | 1 | ||
rs59646751 | 15 | 98733292 | intron variant | G/T | snv | 0.31 | 1 | ||||
rs11858316 | 0.925 | 0.120 | 15 | 98705800 | intron variant | C/T | snv | 0.50 | 1 | ||
rs12361687 | 11 | 9868505 | intron variant | G/A | snv | 0.27 | 1 | ||||
rs12428035 | 13 | 95648618 | upstream gene variant | C/A;T | snv | 3 | |||||
rs4918943 | 10 | 95519165 | intron variant | G/A | snv | 0.23 | 1 | ||||
rs7326821 | 13 | 95415950 | intergenic variant | A/G | snv | 0.15 | 1 | ||||
rs35353426 | 8 | 9439736 | upstream gene variant | C/G;T | snv | 1 | |||||
rs7543734 | 1 | 93585354 | intron variant | G/A;C | snv | 1 | |||||
rs7012814 | 8 | 9315848 | intron variant | G/A;T | snv | 2 | |||||
rs7012637 | 8 | 9315699 | intron variant | G/A;C | snv | 3 | |||||
rs913423 | 10 | 93085279 | intergenic variant | G/A | snv | 0.53 | 2 | ||||
rs4418728 | 10 | 93079967 | downstream gene variant | G/T | snv | 0.42 | 8 | ||||
rs2068888 | 10 | 93079885 | downstream gene variant | G/A | snv | 0.42 | 5 | ||||
rs856534 | 10 | 93050908 | intron variant | G/A | snv | 0.51 | 1 | ||||
rs17184313 | 14 | 92635906 | intron variant | C/A;G;T | snv | 2 | |||||
rs35629566 | 14 | 92605972 | intron variant | C/G | snv | 0.12 | 2 | ||||
rs7006504 | 8 | 9216713 | intron variant | T/C | snv | 0.32 | 1 | ||||
rs13269272 | 8 | 92166732 | intergenic variant | T/A | snv | 0.10 | 1 | ||||
rs117243822 | 6 | 89852962 | intron variant | T/C | snv | 1.1E-02 | 1 | ||||
rs7187910 | 16 | 89671938 | non coding transcript exon variant | A/C;G | snv | 1 |