Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10519198 | 0.925 | 0.080 | 15 | 78450412 | intron variant | C/A;G | snv | 2 | |||
rs11638372 | 0.925 | 0.080 | 15 | 78691217 | intron variant | C/A;G;T | snv | 0.28 | 5 | ||
rs1235162 | 0.827 | 0.280 | 6 | 29569447 | intron variant | A/G | snv | 6.0E-02 | 6 | ||
rs12441998 | 0.925 | 0.080 | 15 | 78637030 | intron variant | G/A | snv | 0.63 | 3 | ||
rs12594247 | 0.925 | 0.080 | 15 | 78654291 | intron variant | C/T | snv | 0.14 | 3 | ||
rs12910984 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 4 | |||
rs12914385 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 13 | |||
rs1316971 | 0.925 | 0.080 | 15 | 78638168 | intron variant | A/G;T | snv | 0.62 | 3 | ||
rs13314271 | 0.925 | 0.080 | 3 | 189639813 | intron variant | T/C | snv | 0.45 | 2 | ||
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 18 | ||
rs2523987 | 0.827 | 0.280 | 6 | 30112216 | intron variant | A/C | snv | 9.2E-02 | 5 | ||
rs259919 | 0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 | 6 | ||
rs259940 | 0.925 | 0.080 | 6 | 30044157 | intron variant | A/G | snv | 0.23 | 2 | ||
rs2656069 | 0.882 | 0.080 | 15 | 78453365 | intron variant | C/G;T | snv | 4 | |||
rs2734986 | 0.827 | 0.160 | 6 | 29850791 | intron variant | T/C | snv | 0.10 | 3 | ||
rs3117143 | 0.882 | 0.160 | 6 | 29063365 | intron variant | C/A | snv | 5.2E-02 | 4 | ||
rs3117582 | 0.716 | 0.440 | 6 | 31652743 | intron variant | T/G | snv | 7.1E-02 | 8 | ||
rs3129791 | 0.827 | 0.280 | 6 | 28986516 | intron variant | G/A | snv | 5.3E-02 | 5 | ||
rs3130380 | 0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 | 10 | ||
rs3131379 | 0.752 | 0.440 | 6 | 31753256 | intron variant | G/A | snv | 6.4E-02 | 7.9E-02 | 6 | |
rs3132610 | 0.807 | 0.280 | 6 | 30576624 | intron variant | A/G | snv | 7.4E-02 | 6 | ||
rs3132685 | 0.807 | 0.320 | 6 | 29978172 | intron variant | G/A;T | snv | 6 | |||
rs31489 | 0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 | 5 | ||
rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 17 | ||
rs4380028 | 0.807 | 0.120 | 15 | 78818751 | intron variant | C/T | snv | 0.34 | 4 |