Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1007323 | 6 | 10953011 | intron variant | T/A;G | snv | 1 | |||||
rs10792320 | 11 | 61978819 | intergenic variant | A/C;T | snv | 1 | |||||
rs12199131 | 6 | 10932336 | intron variant | G/A;T | snv | 1 | |||||
rs1225717 | 6 | 10978007 | intron variant | A/G;T | snv | 1 | |||||
rs12472274 | 2 | 238186781 | non coding transcript exon variant | G/A;T | snv | 1 | |||||
rs12526913 | 6 | 11082691 | downstream gene variant | A/G;T | snv | 1 | |||||
rs1321536 | 6 | 11018579 | intron variant | T/A;G | snv | 1 | |||||
rs1323739 | 6 | 11004328 | intron variant | C/G;T | snv | 1 | |||||
rs174589 | 11 | 61848331 | intron variant | C/G;T | snv | 0.19 | 1 | ||||
rs17764592 | 6 | 11002911 | intron variant | A/C;G | snv | 1 | |||||
rs198428 | 11 | 61722233 | intron variant | A/G;T | snv | 1 | |||||
rs2028062 | 11 | 61978481 | intergenic variant | G/A;C | snv | 1 | |||||
rs2235093 | 11 | 61897650 | 3 prime UTR variant | A/G;T | snv | 1 | |||||
rs2945816 | 11 | 56094615 | downstream gene variant | T/C | snv | 1 | |||||
rs3117181 | 6 | 32103240 | intron variant | C/A;G;T | snv | 1 | |||||
rs3758977 | 11 | 61969772 | upstream gene variant | T/A;G | snv | 1 | |||||
rs4532436 | 6 | 10983738 | 3 prime UTR variant | C/A;G;T | snv | 0.54; 5.0E-06 | 1 | ||||
rs4711171 | 6 | 11074114 | intron variant | C/A;T | snv | 1 | |||||
rs4963444 | 11 | 62005870 | regulatory region variant | G/A;T | snv | 1 | |||||
rs569258 | 11 | 61753196 | intron variant | T/C;G | snv | 1 | |||||
rs6918936 | 6 | 10959925 | intron variant | G/A;C | snv | 1 | |||||
rs6920247 | 6 | 10959940 | intron variant | C/A;G | snv | 1 | |||||
rs7337573 | 13 | 60939535 | intron variant | T/C | snv | 1 | |||||
rs7490068 | 13 | 103408045 | intergenic variant | G/A;C | snv | 1 | |||||
rs7774711 | 6 | 10964788 | intron variant | A/G;T | snv | 1 |