Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1003897973 | 0.882 | 0.080 | 19 | 6746039 | missense variant | C/G | snv | 3 | |||
rs1007541 | 0.882 | 0.080 | 2 | 48981895 | intron variant | C/T | snv | 0.16 | 4 | ||
rs1030389 | 0.882 | 0.080 | 15 | 25032641 | non coding transcript exon variant | A/G | snv | 0.41 | 3 | ||
rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 25 | |
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs10426502 | 0.882 | 0.080 | 19 | 4651257 | intron variant | G/A | snv | 6.8E-02 | 3 | ||
rs1042725 | 0.882 | 0.080 | 12 | 65964567 | 3 prime UTR variant | C/T | snv | 0.48 | 7 | ||
rs1045935 | 0.882 | 0.080 | 15 | 25036439 | non coding transcript exon variant | G/A;T | snv | 3 | |||
rs1047840 | 0.708 | 0.280 | 1 | 241878999 | missense variant | G/A | snv | 0.36 | 0.40 | 19 | |
rs1048512 | 0.882 | 0.080 | 1 | 160025108 | 3 prime UTR variant | G/A;T | snv | 0.13 | 3 | ||
rs1048638 | 0.807 | 0.160 | 9 | 35681125 | 3 prime UTR variant | C/A;G | snv | 10 | |||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 71 | ||
rs1048943 | 0.533 | 0.720 | 15 | 74720644 | missense variant | T/A;C;G | snv | 0.11 | 5.9E-02 | 88 | |
rs1049216 | 0.790 | 0.200 | 4 | 184628935 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
rs1058808 | 0.658 | 0.360 | 17 | 39727784 | missense variant | C/G | snv | 0.61 | 0.52 | 27 | |
rs1059234 | 0.790 | 0.120 | 6 | 36685820 | 3 prime UTR variant | C/T | snv | 0.15 | 0.13 | 10 | |
rs1060555 | 0.882 | 0.080 | 19 | 4652810 | 3 prime UTR variant | C/G;T | snv | 3 | |||
rs10802996 | 0.882 | 0.080 | 1 | 241847325 | upstream gene variant | C/A;G | snv | 5 | |||
rs10815144 | 0.882 | 0.080 | 9 | 5010192 | intron variant | G/A | snv | 0.62 | 3 | ||
rs10893506 | 0.882 | 0.080 | 11 | 126406065 | 5 prime UTR variant | T/A;C | snv | 6.4E-06; 0.41 | 5 | ||
rs11064 | 0.807 | 0.120 | 5 | 119393693 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
rs11079454 | 0.882 | 0.080 | 17 | 61679808 | 3 prime UTR variant | T/A;C | snv | 3 | |||
rs1110839 | 0.807 | 0.120 | 2 | 113236840 | non coding transcript exon variant | G/A;C;T | snv | 6 | |||
rs11125 | 0.851 | 0.120 | 14 | 55145121 | missense variant | A/T | snv | 6.5E-02 | 5.7E-02 | 5 |