Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3025053 | 0.925 | 0.120 | 6 | 43785588 | 3 prime UTR variant | G/A | snv | 8.6E-02 | 2 | ||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs3025040 | 0.882 | 0.120 | 6 | 43785314 | 3 prime UTR variant | C/T | snv | 0.15 | 3 | ||
rs1479430148 | 1.000 | 0.120 | 6 | 43784861 | 3 prime UTR variant | A/T | snv | 1 | |||
rs3025039 | 0.576 | 0.720 | 6 | 43784799 | 3 prime UTR variant | C/T | snv | 0.13 | 62 | ||
rs771561387 | 1.000 | 0.080 | 6 | 43784557 | missense variant | C/G;T | snv | 4.0E-06; 1.2E-05 | 2 | ||
rs748984440 | 1.000 | 0.040 | 6 | 43784546 | stop lost | A/C | snv | 4.0E-06 | 2 | ||
rs3025036 | 1.000 | 0.080 | 6 | 43783932 | non coding transcript exon variant | G/A;C;T | snv | 1 | |||
rs3025035 | 0.851 | 0.240 | 6 | 43783622 | non coding transcript exon variant | C/T | snv | 0.14 | 4 | ||
rs3025033 | 0.807 | 0.360 | 6 | 43783338 | non coding transcript exon variant | A/G | snv | 0.18 | 6 | ||
rs3025030 | 0.882 | 0.200 | 6 | 43782850 | non coding transcript exon variant | G/C | snv | 0.13 | 3 | ||
rs140461341 | 6 | 43782078 | missense variant | G/A | snv | 3.6E-05 | 4.2E-05 | 2 | |||
rs752907384 | 0.827 | 0.200 | 6 | 43782077 | missense variant | C/G;T | snv | 8.0E-06 | 6 | ||
rs749491856 | 1.000 | 6 | 43782071 | missense variant | A/C | snv | 1 | ||||
rs1229919945 | 1.000 | 0.040 | 6 | 43782041 | missense variant | T/C | snv | 1 | |||
rs1287276985 | 0.790 | 0.200 | 6 | 43782020 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 7.0E-06 | 7 | |
rs376388064 | 6 | 43782006 | missense variant | C/T | snv | 2.8E-05 | 3.5E-05 | 1 | |||
rs1188254133 | 0.851 | 0.240 | 6 | 43781990 | missense variant | T/G | snv | 7.0E-06 | 4 | ||
rs3025021 | 0.882 | 0.160 | 6 | 43781426 | non coding transcript exon variant | T/C | snv | 0.70 | 4 | ||
rs3025020 | 0.882 | 0.240 | 6 | 43781373 | non coding transcript exon variant | C/T | snv | 0.24 | 3 | ||
rs752153816 | 0.882 | 0.120 | 6 | 43780848 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 | 3 | ||
rs777846438 | 0.925 | 0.240 | 6 | 43780801 | splice region variant | C/T | snv | 4.4E-05 | 6.3E-05 | 2 | |
rs141138308 | 1.000 | 0.040 | 6 | 43780784 | missense variant | C/A;T | snv | 4.0E-06; 2.8E-05 | 1 | ||
rs774265827 | 6 | 43780773 | missense variant | G/A;T | snv | 8.0E-06; 2.0E-05 | 1 | ||||
rs138551969 | 1.000 | 0.040 | 6 | 43780749 | missense variant | A/G | snv | 1.2E-05 | 3.5E-05 | 4 |