Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs709399 | 0.882 | 0.080 | 14 | 103701208 | 3 prime UTR variant | G/A | snv | 0.59 | 0.61 | 3 | |
rs747463591 | 0.882 | 0.080 | 10 | 59906391 | missense variant | C/A;G;T | snv | 4.9E-06; 9.9E-06 | 3 | ||
rs779791579 | 0.882 | 0.080 | 9 | 95508325 | missense variant | G/C | snv | 7.8E-04 | 6.1E-04 | 3 | |
rs78929565 | 0.882 | 0.080 | 4 | 55539035 | intron variant | C/A;T | snv | 3 | |||
rs183334241 | 0.925 | 0.080 | 18 | 75288186 | missense variant | G/A;C | snv | 1.6E-04 | 2 | ||
rs200817352 | 1.000 | 0.080 | 2 | 113220126 | missense variant | G/A;C | snv | 2.0E-03; 4.0E-06 | 2 | ||
rs373646414 | 1.000 | 0.080 | 14 | 95132574 | missense variant | T/C | snv | 1.6E-05 | 5.6E-05 | 2 | |
rs377767414 | 0.925 | 0.080 | 10 | 43118397 | missense variant | G/A | snv | 2 | |||
rs78081605 | 0.925 | 0.080 | 18 | 75288051 | missense variant | G/C | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs11214077 | 0.752 | 0.120 | 11 | 112087953 | missense variant | A/G | snv | 6.6E-03 | 6.7E-03 | 12 | |
rs34677591 | 0.742 | 0.120 | 11 | 112086941 | missense variant | G/A | snv | 7.5E-03 | 7.0E-03 | 12 | |
rs116909374 | 0.776 | 0.120 | 14 | 36269155 | regulatory region variant | C/T | snv | 2.3E-02 | 11 | ||
rs33917957 | 0.790 | 0.120 | 7 | 116700208 | missense variant | A/G | snv | 2.7E-02 | 1.8E-02 | 10 | |
rs778212685 | 0.827 | 0.120 | 22 | 28712015 | missense variant | C/A;G;T | snv | 4.0E-06 | 8 | ||
rs360718 | 0.827 | 0.120 | 11 | 112164016 | 5 prime UTR variant | A/C | snv | 0.26 | 5 | ||
rs786203472 | 0.827 | 0.120 | 22 | 28719414 | start lost | T/C | snv | 5 | |||
rs863224748 | 0.827 | 0.120 | 22 | 28734721 | start lost | T/C | snv | 5 | |||
rs1946519 | 0.851 | 0.120 | 11 | 112164784 | intron variant | A/C | snv | 0.60 | 4 | ||
rs377767427 | 0.882 | 0.120 | 10 | 43120114 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
rs147394161 | 0.925 | 0.120 | 1 | 21598453 | missense variant | T/C | snv | 9.5E-03 | 1.0E-02 | 2 | |
rs1057519736 | 0.752 | 0.160 | 15 | 90088605 | missense variant | C/G | snv | 13 | |||
rs77709286 | 0.752 | 0.160 | 10 | 43114502 | missense variant | C/G | snv | 4.0E-06 | 12 | ||
rs12628 | 0.776 | 0.160 | 11 | 534242 | synonymous variant | A/G | snv | 0.32 | 0.34 | 10 | |
rs1867277 | 0.776 | 0.160 | 9 | 97853632 | 5 prime UTR variant | A/G | snv | 0.63 | 10 | ||
rs1297812518 | 0.763 | 0.160 | 14 | 103707168 | missense variant | G/A | snv | 1.3E-05 | 1.4E-05 | 9 |