Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12662634 | 6 | 11073958 | intron variant | G/A | snv | 0.17 | 1 | ||||
rs1321535 | 6 | 11075793 | intron variant | T/G | snv | 0.41 | 1 | ||||
rs17675322 | 6 | 11058952 | intron variant | T/A | snv | 0.59 | 1 | ||||
rs17764682 | 6 | 11058582 | intron variant | A/C | snv | 0.24 | 1 | ||||
rs2147041 | 6 | 11050290 | intron variant | A/G | snv | 0.53 | 1 | ||||
rs4711170 | 6 | 11070201 | intron variant | C/A | snv | 0.17 | 1 | ||||
rs4711171 | 6 | 11074114 | intron variant | C/A;T | snv | 1 | |||||
rs4713165 | 6 | 11074069 | intron variant | T/C | snv | 0.41 | 1 | ||||
rs6900220 | 6 | 11064905 | intron variant | T/C | snv | 0.53 | 1 | ||||
rs9295763 | 6 | 11044959 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||||
rs9295764 | 6 | 11044963 | non coding transcript exon variant | A/G | snv | 0.59 | 1 | ||||
rs9368564 | 6 | 11060050 | intron variant | A/G;T | snv | 1 | |||||
rs9393903 | 6 | 11042676 | intron variant | G/A | snv | 0.18 | 3 | ||||
rs9393915 | 6 | 11072089 | intron variant | C/T | snv | 0.23 | 1 | ||||
rs9468304 | 1.000 | 0.040 | 6 | 11041932 | intron variant | G/A | snv | 0.19 | 2 |