Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131691036 | 0.851 | 0.080 | 17 | 7675207 | frameshift variant | GCA/CC | delins | 8 | |||
rs2287499 | 0.925 | 0.080 | 17 | 7688850 | missense variant | C/G;T | snv | 0.20 | 4 | ||
rs1064795369 | 0.882 | 0.080 | 17 | 7673791 | missense variant | A/C;G | snv | 3 | |||
rs1159579789 | 0.925 | 0.080 | 17 | 7673578 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
rs587781433 | 0.925 | 0.080 | 17 | 7674197 | missense variant | T/C;G | snv | 3 | |||
rs1064794312 | 0.925 | 0.080 | 17 | 7674278 | missense variant | A/G | snv | 8.0E-06 | 2 | ||
rs1177881399 | 0.925 | 0.080 | 17 | 7673557 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs1237722021 | 0.925 | 0.080 | 17 | 7676194 | missense variant | C/A | snv | 7.0E-06 | 2 | ||
rs587782646 | 0.925 | 0.080 | 17 | 7676576 | missense variant | C/G | snv | 4.0E-06 | 2 | ||
rs1288373809 | 0.882 | 0.120 | 17 | 7673255 | synonymous variant | G/A | snv | 5.3E-06 | 5 | ||
rs375275361 | 0.827 | 0.120 | 17 | 7675054 | missense variant | A/G;T | snv | 1.2E-05; 4.0E-06 | 5 | ||
rs779196500 | 0.882 | 0.120 | 17 | 7675187 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs372201428 | 0.882 | 0.120 | 17 | 7676181 | missense variant | G/A;C | snv | 1.2E-05 | 3 | ||
rs587782144 | 0.807 | 0.160 | 17 | 7675139 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 8 | ||
rs1625895 | 0.752 | 0.200 | 17 | 7674797 | non coding transcript exon variant | T/A;C;G | snv | 9.1E-06; 0.86; 4.5E-06 | 13 | ||
rs587782596 | 0.807 | 0.200 | 17 | 7675071 | missense variant | G/A;T | snv | 7 | |||
rs1457582183 | 0.827 | 0.200 | 17 | 7673608 | missense variant | G/A;C | snv | 7.0E-06 | 5 | ||
rs1800371 | 0.742 | 0.240 | 17 | 7676230 | missense variant | G/A;T | snv | 1.2E-03 | 15 | ||
rs1800372 | 0.752 | 0.240 | 17 | 7674892 | synonymous variant | T/A;C | snv | 1.3E-02 | 15 | ||
rs587780071 | 0.732 | 0.240 | 17 | 7674951 | missense variant | G/A | snv | 15 | |||
rs1057520006 | 0.752 | 0.240 | 17 | 7673799 | missense variant | A/C;G;T | snv | 14 | |||
rs397516435 | 0.851 | 0.280 | 17 | 7674945 | stop gained | G/A;C | snv | 4.0E-06 | 6 | ||
rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 57 | ||
rs121912664 | 0.630 | 0.320 | 17 | 7670699 | missense variant | C/A;G;T | snv | 1.2E-05 | 44 | ||
rs375874539 | 0.732 | 0.320 | 17 | 7674237 | missense variant | G/A;C | snv | 15 |