Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2073643 | 1.000 | 0.080 | 5 | 132387596 | intron variant | T/C | snv | 0.46 | 4 | ||
rs1158867 | 1.000 | 0.080 | 2 | 127419801 | splice region variant | C/T | snv | 0.51 | 3 | ||
rs3859192 | 0.925 | 0.080 | 17 | 39972395 | intron variant | C/T | snv | 0.42 | 3 | ||
rs4795400 | 0.925 | 0.080 | 17 | 39910767 | intron variant | C/T | snv | 0.36 | 3 | ||
rs8069176 | 0.882 | 0.080 | 17 | 39900944 | downstream gene variant | G/A;T | snv | 3 | |||
rs907092 | 0.925 | 0.080 | 17 | 39766006 | synonymous variant | G/A | snv | 0.41 | 0.36 | 3 | |
rs10056340 | 0.925 | 0.080 | 5 | 110854353 | intergenic variant | T/G | snv | 0.31 | 2 | ||
rs10173081 | 1.000 | 0.080 | 2 | 102340888 | intron variant | C/T | snv | 0.18 | 2 | ||
rs10189629 | 1.000 | 0.080 | 2 | 102263004 | regulatory region variant | C/A | snv | 0.15 | 2 | ||
rs10192157 | 1.000 | 0.080 | 2 | 102351896 | missense variant | C/T | snv | 0.34 | 0.46 | 2 | |
rs10206753 | 1.000 | 0.080 | 2 | 102351902 | missense variant | T/C;G | snv | 0.34; 4.0E-06 | 2 | ||
rs1043828 | 1.000 | 0.080 | 5 | 111128310 | 3 prime UTR variant | T/C;G | snv | 2 | |||
rs11078927 | 0.925 | 0.080 | 17 | 39908152 | intron variant | C/T | snv | 0.40 | 0.35 | 2 | |
rs11674302 | 1.000 | 0.080 | 2 | 102270668 | intergenic variant | T/C | snv | 0.16 | 2 | ||
rs11692065 | 1.000 | 0.080 | 2 | 102267515 | intergenic variant | C/T | snv | 0.15 | 2 | ||
rs12734001 | 1.000 | 0.080 | 1 | 202421786 | intron variant | C/T | snv | 3.5E-05 | 2 | ||
rs13408569 | 1.000 | 0.080 | 2 | 102338596 | intron variant | G/C | snv | 0.18 | 2 | ||
rs13408661 | 1.000 | 0.080 | 2 | 102338622 | intron variant | G/A | snv | 0.18 | 2 | ||
rs1362348 | 1.000 | 0.080 | 2 | 102368164 | intron variant | C/G | snv | 0.45 | 2 | ||
rs17454584 | 0.851 | 0.080 | 4 | 122432277 | downstream gene variant | A/G | snv | 0.17 | 2 | ||
rs17498196 | 1.000 | 0.080 | 9 | 6237547 | intron variant | A/C;G | snv | 2 | |||
rs2066362 | 1.000 | 0.080 | 9 | 6219176 | intron variant | G/C;T | snv | 2 | |||
rs2381416 | 1.000 | 0.080 | 9 | 6193455 | upstream gene variant | C/A | snv | 0.65 | 2 | ||
rs3771166 | 1.000 | 0.080 | 2 | 102369762 | intron variant | G/A;T | snv | 2 | |||
rs3771175 | 0.925 | 0.080 | 2 | 102343750 | 3 prime UTR variant | T/A | snv | 0.18 | 2 |