Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9967983 | 0.925 | 0.080 | 21 | 31665169 | intron variant | A/T | snv | 0.47 | 2 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs9915936 | 0.827 | 0.120 | 17 | 65537671 | synonymous variant | T/C | snv | 0.90 | 0.90 | 5 | |
rs9900242 | 0.925 | 0.080 | 17 | 71139490 | intron variant | G/A | snv | 0.32 | 2 | ||
rs9852810 | 0.882 | 0.080 | 3 | 37027478 | intron variant | G/A | snv | 0.35 | 3 | ||
rs9832989 | 1.000 | 0.080 | 3 | 133982979 | intron variant | A/G | snv | 1.4E-02 | 1 | ||
rs980171 | 0.925 | 0.080 | 8 | 127042277 | intron variant | A/G | snv | 0.45 | 2 | ||
rs976306779 | 0.851 | 0.080 | X | 67545492 | missense variant | C/A;T | snv | 6.6E-06 | 8 | ||
rs968098233 | 0.882 | 0.200 | X | 67546162 | missense variant | T/C | snv | 3 | |||
rs9666607 | 0.925 | 0.080 | 11 | 35204608 | missense variant | A/G;T | snv | 0.74 | 2 | ||
rs9658655 | 0.925 | 0.080 | 14 | 92931686 | missense variant | G/C | snv | 0.13 | 0.12 | 2 | |
rs9651118 | 0.683 | 0.480 | 1 | 11802157 | intron variant | T/C | snv | 0.18 | 20 | ||
rs9644474 | 1.000 | 0.080 | 8 | 136150901 | intron variant | C/T | snv | 0.71 | 1 | ||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs9625483 | 1.000 | 0.080 | 22 | 28492951 | intron variant | G/A | snv | 1.9E-02 | 1 | ||
rs9623117 | 0.851 | 0.200 | 22 | 40056115 | intron variant | T/C | snv | 0.38 | 4 | ||
rs9608380 | 0.925 | 0.080 | 22 | 25226475 | intron variant | C/T | snv | 0.12 | 2 | ||
rs9600079 | 0.925 | 0.080 | 13 | 73154002 | intergenic variant | G/T | snv | 0.46 | 5 | ||
rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
rs946993012 | 0.925 | 0.080 | 12 | 117331056 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs9469899 | 1.000 | 0.080 | 6 | 34825347 | intron variant | G/A | snv | 0.46 | 1 | ||
rs9443189 | 1.000 | 0.080 | 6 | 75786165 | intron variant | A/G | snv | 0.26 | 1 | ||
rs9393682 | 0.925 | 0.080 | 6 | 26056822 | upstream gene variant | C/T | snv | 9.8E-02 | 2 | ||
rs9388766 | 0.925 | 0.080 | 6 | 130033710 | intron variant | T/C | snv | 0.65 | 3 | ||
rs9375701 | 0.827 | 0.160 | 6 | 130062912 | intron variant | C/T | snv | 0.53 | 6 |