Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10832027 | 11 | 13335636 | intron variant | G/A | snv | 0.67 | 5 | ||||
rs1126930 | 12 | 49005349 | missense variant | G/C | snv | 2.1E-02 | 2.1E-02 | 5 | |||
rs1129555 | 10 | 112150963 | 3 prime UTR variant | A/G | snv | 0.71 | 5 | ||||
rs114165349 | 1 | 26695422 | intron variant | G/C | snv | 1.7E-02 | 5 | ||||
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 5 | ||||
rs127430 | 20 | 58589799 | intron variant | A/G;T | snv | 5 | |||||
rs17199964 | 4 | 101786634 | intron variant | G/A;C | snv | 5 | |||||
rs2068888 | 10 | 93079885 | downstream gene variant | G/A | snv | 0.42 | 5 | ||||
rs2249105 | 2 | 65060762 | intron variant | A/G | snv | 0.40 | 5 | ||||
rs2845885 | 11 | 64101590 | intron variant | C/T | snv | 0.87 | 5 | ||||
rs438811 | 19 | 44913484 | non coding transcript exon variant | C/T | snv | 0.29 | 5 | ||||
rs4665710 | 2 | 20998163 | downstream gene variant | A/C | snv | 0.76 | 5 | ||||
rs661171 | 11 | 110145794 | intron variant | T/G | snv | 0.69 | 5 | ||||
rs7096937 | 10 | 112190660 | intron variant | T/C | snv | 0.72 | 5 | ||||
rs72959041 | 6 | 127133748 | intron variant | G/A | snv | 3.2E-02 | 5 | ||||
rs77960347 | 18 | 49583585 | missense variant | A/C;G | snv | 4.0E-06; 8.7E-03 | 5 | ||||
rs7890572 | X | 29622701 | intron variant | A/G | snv | 9.3E-02 | 5 | ||||
rs79598313 | 1 | 26958422 | intron variant | C/A;T | snv | 5 | |||||
rs9991328 | 4 | 88791970 | intron variant | C/T | snv | 0.53 | 5 | ||||
rs10054063 | 5 | 173965395 | downstream gene variant | A/T | snv | 0.26 | 4 | ||||
rs1011731 | 1 | 172377408 | intron variant | G/A | snv | 0.46 | 4 | ||||
rs10127775 | 1 | 230160042 | intron variant | A/G;T | snv | 4 | |||||
rs10185855 | 2 | 101025798 | intron variant | A/G | snv | 0.35 | 4 | ||||
rs1041968 | 2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 | 4 | |||
rs1065853 | 19 | 44909976 | non coding transcript exon variant | G/A;C;T | snv | 4 |