Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs174574 | 1.000 | 0.080 | 11 | 61832870 | intron variant | A/C | snv | 0.55 | 2 | ||
rs1535 | 0.752 | 0.240 | 11 | 61830500 | intron variant | A/G | snv | 0.31 | 10 | ||
rs2851682 | 11 | 61848540 | intron variant | A/G | snv | 9.9E-02 | 5 | ||||
rs2072114 | 1.000 | 0.080 | 11 | 61837743 | intron variant | A/G | snv | 0.19 | 0.16 | 2 | |
rs2845573 | 1.000 | 0.040 | 11 | 61834436 | intron variant | A/G | snv | 9.7E-02 | 2 | ||
rs695867 | 11 | 61793816 | intron variant | A/G | snv | 2.6E-02 | 1 | ||||
rs17156426 | 11 | 61841851 | intron variant | A/G;T | snv | 2 | |||||
rs2524299 | 11 | 61837310 | intron variant | A/T | snv | 0.17 | 2 | ||||
rs2727271 | 11 | 61835886 | intron variant | A/T | snv | 0.12 | 2 | ||||
rs174575 | 1.000 | 0.040 | 11 | 61834531 | intron variant | C/G | snv | 0.25 | 2 | ||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs174589 | 11 | 61848331 | intron variant | C/G;T | snv | 0.19 | 1 | ||||
rs174570 | 0.882 | 0.200 | 11 | 61829740 | intron variant | C/T | snv | 0.15 | 10 | ||
rs174583 | 0.807 | 0.320 | 11 | 61842278 | intron variant | C/T | snv | 0.35 | 5 | ||
rs174556 | 0.925 | 0.160 | 11 | 61813163 | intron variant | C/T | snv | 0.26 | 3 | ||
rs968567 | 0.851 | 0.240 | 11 | 61828092 | intron variant | C/T | snv | 0.11 | 3 | ||
rs17156442 | 11 | 61846551 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs174579 | 11 | 61838141 | intron variant | C/T | snv | 0.16 | 2 | ||||
rs2727270 | 11 | 61835765 | intron variant | C/T | snv | 0.12 | 2 | ||||
rs7935946 | 11 | 61848070 | 5 prime UTR variant | C/T | snv | 0.11 | 2 | ||||
rs174616 | 1.000 | 0.080 | 11 | 61861650 | intron variant | G/A | snv | 0.51 | 2 | ||
rs2526678 | 11 | 61856321 | non coding transcript exon variant | G/A | snv | 8.6E-02 | 2 | ||||
rs174597 | 11 | 61853568 | intron variant | G/A;C;T | snv | 2 | |||||
rs174585 | 11 | 61844222 | intron variant | G/A;T | snv | 2 | |||||
rs17764324 | 11 | 61867616 | downstream gene variant | G/A;T | snv | 2 |