Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3025020 | 0.882 | 0.240 | 6 | 43781373 | non coding transcript exon variant | C/T | snv | 0.24 | 3 | ||
rs3025040 | 0.882 | 0.120 | 6 | 43785314 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
rs374057152 | 0.925 | 0.200 | 6 | 43777592 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs3025021 | 0.882 | 0.160 | 6 | 43781426 | non coding transcript exon variant | T/C | snv | 0.70 | 3 | ||
rs1413711 | 0.882 | 0.200 | 6 | 43772941 | intron variant | T/A;C | snv | 3 | |||
rs3024997 | 0.882 | 0.120 | 6 | 43777370 | non coding transcript exon variant | G/A | snv | 0.31 | 3 | ||
rs766474822 | 0.925 | 0.080 | 6 | 43770990 | missense variant | G/A | snv | 1.4E-05 | 2.1E-05 | 2 | |
rs1305315912 | 1.000 | 0.080 | 6 | 43770736 | synonymous variant | C/T | snv | 2 | |||
rs3025053 | 0.925 | 0.120 | 6 | 43785588 | 3 prime UTR variant | G/A | snv | 8.6E-02 | 2 | ||
rs748352475 | 0.925 | 0.160 | 6 | 43777546 | missense variant | C/G | snv | 1.2E-05 | 7.0E-06 | 2 | |
rs1243046808 | 0.925 | 0.160 | 6 | 43770758 | missense variant | C/G;T | snv | 2.0E-05; 9.8E-06 | 2 | ||
rs777846438 | 0.925 | 0.240 | 6 | 43780801 | splice region variant | C/T | snv | 4.4E-05 | 6.3E-05 | 2 | |
rs1212415280 | 6 | 43771130 | missense variant | G/T | snv | 2.1E-05 | 2 | ||||
rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
rs140461341 | 6 | 43782078 | missense variant | G/A | snv | 3.6E-05 | 4.2E-05 | 2 | |||
rs1365501228 | 1.000 | 0.080 | 6 | 43770732 | missense variant | C/T | snv | 1.4E-05 | 2 | ||
rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 | ||||
rs1404013760 | 1.000 | 0.040 | 6 | 43771137 | missense variant | G/C | snv | 8.9E-06 | 1 | ||
rs3025036 | 1.000 | 0.080 | 6 | 43783932 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
rs1421145908 | 6 | 43777618 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
rs541717889 | 6 | 43770888 | missense variant | G/C | snv | 2.1E-05 | 1 | ||||
rs1201894677 | 6 | 43770833 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
rs735286 | 6 | 43776884 | non coding transcript exon variant | C/T | snv | 0.23 | 1 | ||||
rs3025010 | 6 | 43779840 | non coding transcript exon variant | T/C;G | snv | 1 |