Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4795519 | 1.000 | 0.080 | 17 | 27214252 | intergenic variant | A/C | snv | 0.43 | 1 | ||
rs1239681664 | 0.716 | 0.320 | 9 | 104818690 | synonymous variant | A/G | snv | 7.0E-06 | 15 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs4148356 | 0.851 | 0.120 | 16 | 16083418 | missense variant | G/A | snv | 2.3E-02 | 1.3E-02 | 4 | |
rs45511401 | 0.851 | 0.120 | 16 | 16079375 | missense variant | G/T | snv | 3.8E-02 | 3.6E-02 | 4 | |
rs3740066 | 0.724 | 0.440 | 10 | 99844450 | missense variant | C/G;T | snv | 2.4E-05; 0.34 | 20 | ||
rs2273697 | 0.776 | 0.360 | 10 | 99804058 | missense variant | G/A | snv | 0.19 | 0.19 | 11 | |
rs717620 | 0.763 | 0.240 | 10 | 99782821 | 5 prime UTR variant | C/T | snv | 0.17 | 0.15 | 10 | |
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs121913459 | 0.672 | 0.160 | 9 | 130872896 | missense variant | C/T | snv | 25 | |||
rs387906517 | 0.827 | 0.120 | 9 | 130862919 | missense variant | G/A | snv | 6 | |||
rs121913448 | 0.827 | 0.120 | 9 | 130862976 | missense variant | G/A | snv | 5 | |||
rs121913461 | 0.851 | 0.120 | 9 | 130862970 | missense variant | T/C | snv | 5 | |||
rs1057519773 | 0.851 | 0.160 | 9 | 130872901 | missense variant | T/A;C;G | snv | 4 | |||
rs121913451 | 0.851 | 0.160 | 9 | 130872903 | missense variant | C/A;G | snv | 4 | |||
rs121913452 | 0.851 | 0.080 | 9 | 130873027 | missense variant | T/A;C;G | snv | 4 | |||
rs1057519771 | 1.000 | 0.080 | 9 | 130872201 | missense variant | G/C | snv | 2 | |||
rs121913454 | 0.925 | 0.080 | 9 | 130874969 | missense variant | A/G | snv | 2 | |||
rs121913460 | 0.925 | 0.080 | 9 | 130862971 | missense variant | A/T | snv | 2 | |||
rs1314838108 | 0.925 | 0.160 | 9 | 130854977 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs1057519758 | 1.000 | 0.080 | 9 | 130872153 | missense variant | T/G | snv | 1 | |||
rs1057519772 | 1.000 | 0.080 | 9 | 130872895 | missense variant | A/G | snv | 1 | |||
rs1057519774 | 1.000 | 0.080 | 9 | 130872902 | missense variant | T/G | snv | 1 |