Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6721961 | 0.672 | 0.520 | 2 | 177265309 | intron variant | T/C;G | snv | 0.89 | 24 | ||
rs35652124 | 0.790 | 0.320 | 2 | 177265345 | intron variant | T/C | snv | 0.29 | 8 | ||
rs26907 | 0.882 | 0.240 | 5 | 81069496 | intron variant | G/A;T | snv | 3 | |||
rs398123108 | 0.925 | 0.200 | X | 153743211 | intron variant | G/A;T | snv | 3 | |||
rs4893819 | 1.000 | 0.160 | 2 | 177266406 | intron variant | C/T | snv | 0.55 | 1 | ||
rs1170974058 | 1.000 | 0.160 | X | 153743495 | stop gained | C/A;T | snv | 2.8E-05 | 1 | ||
rs128624221 | 1.000 | 0.160 | X | 153736510 | stop gained | C/T | snv | 1 | |||
rs128624222 | 1.000 | 0.160 | X | 153737192 | stop gained | G/A;T | snv | 2.2E-05 | 1 | ||
rs1557054210 | 1.000 | 0.160 | X | 153736390 | stop gained | C/T | snv | 1 | |||
rs1569541000 | 1.000 | 0.160 | X | 153736126 | stop gained | A/T | snv | 1 | |||
rs782266592 | 1.000 | 0.160 | X | 153736156 | stop gained | G/C;T | snv | 2.7E-05 | 2.8E-05 | 1 | |
rs797044726 | 1.000 | 0.160 | X | 153736408 | stop gained | C/T | snv | 1 | |||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs4880 | 0.500 | 0.840 | 6 | 159692840 | missense variant | A/G | snv | 0.48 | 0.47 | 131 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs738409 | 0.557 | 0.720 | 22 | 43928847 | missense variant | C/G | snv | 0.28 | 0.22 | 88 | |
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
rs58542926 | 0.630 | 0.440 | 19 | 19268740 | missense variant | C/T | snv | 6.5E-02 | 5.8E-02 | 42 | |
rs17107315 | 0.620 | 0.440 | 5 | 147828115 | missense variant | T/C | snv | 9.1E-03 | 8.2E-03 | 40 | |
rs1223231582 | 0.677 | 0.280 | 7 | 142750639 | missense variant | A/G | snv | 7.0E-06 | 24 | ||
rs1557055405 | 0.807 | 0.400 | X | 153743532 | missense variant | T/A | snv | 21 |