Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs145640112 | 0.925 | 0.080 | 4 | 186250267 | missense variant | A/C;G | snv | 1.8E-04; 4.0E-06 | 2 | ||
rs4253373 | 0.925 | 0.080 | 4 | 186250250 | missense variant | C/A | snv | 6.7E-04 | 2.5E-03 | 2 | |
rs301640 | 0.925 | 0.080 | 13 | 60885853 | intron variant | C/G;T | snv | 2 | |||
rs12437854 | 0.925 | 0.080 | 15 | 93598604 | intron variant | T/G | snv | 0.10 | 2 | ||
rs17709344 | 0.925 | 0.080 | 15 | 93608310 | intron variant | G/A | snv | 4.0E-02 | 2 | ||
rs9395890 | 0.925 | 0.080 | 6 | 53956196 | intron variant | G/A;T | snv | 2 | |||
rs9298190 | 0.925 | 0.080 | 8 | 71932099 | intron variant | T/C | snv | 0.36 | 2 | ||
rs2413396 | 0.925 | 0.080 | 22 | 36312039 | intron variant | C/G;T | snv | 0.88 | 2 | ||
rs115489112 | 0.925 | 0.080 | 19 | 35830918 | missense variant | G/A | snv | 4.3E-04 | 1.6E-03 | 2 | |
rs146400394 | 0.925 | 0.080 | 19 | 35842486 | missense variant | C/T | snv | 6.8E-05 | 4.9E-05 | 2 | |
rs10808565 | 0.925 | 0.080 | 8 | 127995166 | non coding transcript exon variant | C/T | snv | 0.31 | 2 | ||
rs6954996 | 0.925 | 0.080 | 7 | 6401627 | non coding transcript exon variant | G/A;T | snv | 2 | |||
rs702483 | 0.925 | 0.080 | 7 | 6387310 | intron variant | C/A;T | snv | 0.54 | 2 | ||
rs836488 | 0.925 | 0.080 | 7 | 6380162 | intron variant | C/T | snv | 0.13 | 2 | ||
rs9374 | 0.925 | 0.080 | 7 | 6402740 | 3 prime UTR variant | G/A | snv | 0.18 | 2 | ||
rs12431381 | 0.925 | 0.080 | 14 | 59643053 | intron variant | T/C | snv | 0.35 | 2 | ||
rs2802723 | 0.925 | 0.080 | 1 | 243335010 | intron variant | T/C;G | snv | 2 | |||
rs2838302 | 0.925 | 0.080 | 21 | 43419273 | intron variant | A/G | snv | 1.0E-01 | 2 | ||
rs183962941 | 0.925 | 0.080 | 16 | 20343125 | intron variant | G/A | snv | 1.1E-02 | 2 | ||
rs12197043 | 0.882 | 0.160 | 6 | 149130141 | regulatory region variant | A/G | snv | 0.37 | 3 | ||
rs1670754 | 0.882 | 0.160 | 4 | 32263375 | intergenic variant | G/A | snv | 0.24 | 3 | ||
rs4897081 | 0.882 | 0.160 | 6 | 149115402 | upstream gene variant | G/A;T | snv | 3 | |||
rs8014363 | 0.882 | 0.160 | 14 | 53964857 | downstream gene variant | C/T | snv | 0.61 | 3 | ||
rs1162592300 | 0.925 | 0.080 | 4 | 73412045 | missense variant | G/A | snv | 3 | |||
rs3759126 | 0.882 | 0.080 | 12 | 49950079 | upstream gene variant | A/G | snv | 0.23 | 3 |