Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs311686 | 1.000 | 0.040 | 6 | 73416152 | missense variant | A/G | snv | 0.52 | 0.48 | 1 | |
rs751273816 | 1.000 | 0.040 | 1 | 47373057 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs12294076 | 1.000 | 0.040 | 11 | 103256336 | intron variant | T/C | snv | 6.8E-02 | 1 | ||
rs7675690 | 1.000 | 0.040 | 4 | 74382934 | intron variant | A/G | snv | 9.3E-02 | 1 | ||
rs1045481 | 1.000 | 0.040 | 17 | 744917 | missense variant | G/A;C | snv | 0.20 | 1 | ||
rs865901367 | 1.000 | 0.040 | 22 | 39968124 | missense variant | C/T | snv | 2.1E-05 | 1 | ||
rs534448891 | 1.000 | 0.040 | 16 | 85413567 | intron variant | C/G;T | snv | 6.3E-05 | 1 | ||
rs41553512 | 1.000 | 0.040 | 6 | 32518625 | missense variant | C/T | snv | 0.12 | 4.6E-02 | 1 | |
rs10507172 | 1.000 | 0.040 | 12 | 103949490 | intron variant | G/A | snv | 7.2E-02 | 1 | ||
rs10507173 | 1.000 | 0.040 | 12 | 103950058 | intron variant | A/G | snv | 6.3E-02 | 1 | ||
rs1190662183 | 1.000 | 0.040 | 19 | 10338932 | synonymous variant | C/T | snv | 1 | |||
rs1101998 | 1.000 | 0.040 | 1 | 159029494 | intron variant | C/T | snv | 0.65 | 1 | ||
rs1633256 | 1.000 | 0.040 | 1 | 159032767 | intron variant | A/G | snv | 0.70 | 1 | ||
rs41401746 | 1.000 | 0.040 | 6 | 137219797 | upstream gene variant | AA/- | del | 2.0E-02 | 1 | ||
rs56251346 | 1.000 | 0.040 | 6 | 137199749 | intron variant | C/T | snv | 0.20 | 1 | ||
rs9376269 | 1.000 | 0.040 | 6 | 137218368 | intron variant | C/G | snv | 0.22 | 1 | ||
rs5744247 | 1.000 | 0.040 | 11 | 112155433 | intron variant | G/C | snv | 8.9E-02 | 1 | ||
rs3218255 | 1.000 | 0.040 | 22 | 37148446 | intron variant | G/A | snv | 0.21 | 1 | ||
rs11567764 | 1.000 | 0.040 | 5 | 35873503 | missense variant | G/A;T | snv | 9.5E-03; 4.0E-06 | 1 | ||
rs11246213 | 1.000 | 0.040 | 11 | 612967 | intron variant | A/G | snv | 0.25 | 0.33 | 1 | |
rs10051924 | 1.000 | 0.040 | 5 | 150847077 | 5 prime UTR variant | T/C | snv | 0.21 | 1 | ||
rs12654043 | 1.000 | 0.040 | 5 | 150846533 | 5 prime UTR variant | A/C;G | snv | 1 | |||
rs11958933 | 1.000 | 0.040 | 5 | 25323598 | intron variant | G/A | snv | 0.70 | 1 | ||
rs931924 | 1.000 | 0.040 | 5 | 25321925 | intron variant | C/T | snv | 0.70 | 1 | ||
rs3212220 | 1.000 | 0.040 | 5 | 159327187 | intron variant | C/A | snv | 0.26 | 1 |