Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1010159 | 0.882 | 0.080 | 11 | 121612692 | non coding transcript exon variant | C/T | snv | 0.55 | 0.55 | 3 | |
rs10119 | 0.925 | 0.080 | 19 | 44903416 | 3 prime UTR variant | G/A | snv | 0.28 | 5 | ||
rs10407447 | 1.000 | 0.040 | 19 | 40363275 | intron variant | A/G | snv | 0.20 | 1 | ||
rs104894103 | 0.807 | 0.280 | 9 | 32974495 | stop gained | C/G;T | snv | 4.0E-06; 1.6E-04 | 6 | ||
rs11136000 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 19 | ||
rs111943087 | 0.925 | 0.080 | 5 | 150059725 | missense variant | G/A | snv | 1.4E-05 | 2 | ||
rs11218304 | 0.925 | 0.080 | 11 | 121478402 | intron variant | A/G | snv | 0.30 | 2 | ||
rs1130399 | 1.000 | 0.040 | 6 | 32661978 | missense variant | G/A;T | snv | 0.20 | 1 | ||
rs11556510 | 1.000 | 0.040 | 19 | 44891562 | missense variant | T/G | snv | 9.8E-03 | 1.2E-02 | 1 | |
rs11637611 | 0.851 | 0.160 | 15 | 72259371 | intron variant | C/T | snv | 0.63 | 4 | ||
rs11667768 | 1.000 | 0.040 | 19 | 40348525 | 5 prime UTR variant | C/T | snv | 6.3E-02 | 0.11 | 1 | |
rs11767557 | 0.882 | 0.080 | 7 | 143412046 | intron variant | T/C | snv | 0.18 | 4 | ||
rs1187120 | 0.925 | 0.040 | 6 | 34182850 | intergenic variant | T/C | snv | 0.99 | 3 | ||
rs11887120 | 0.882 | 0.080 | 2 | 25262866 | intron variant | C/T | snv | 0.45 | 4 | ||
rs12053868 | 0.925 | 0.080 | 3 | 190582215 | intron variant | A/G | snv | 8.0E-02 | 2 | ||
rs1207568 | 0.925 | 0.120 | 13 | 33016046 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12344615 | 0.851 | 0.080 | 9 | 83666280 | intron variant | A/C;G | snv | 4 | |||
rs1256049 | 0.645 | 0.560 | 14 | 64257333 | synonymous variant | C/T | snv | 6.7E-02 | 6.3E-02 | 32 | |
rs12752888 | 0.851 | 0.160 | 1 | 54527266 | downstream gene variant | T/C | snv | 0.26 | 4 | ||
rs1334496 | 1.000 | 0.040 | X | 137178554 | intergenic variant | C/A;T | snv | 1 | |||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs1451603364 | 0.925 | 0.120 | 11 | 27658411 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs15009 | 0.925 | 0.080 | 5 | 58454523 | 3 prime UTR variant | C/G | snv | 0.37 | 2 | ||
rs157581 | 0.925 | 0.080 | 19 | 44892457 | synonymous variant | T/C | snv | 0.25 | 0.29 | 3 |