Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs7412 | 0.641 | 0.640 | 19 | 44908822 | missense variant | C/T | snv | 6.2E-02 | 7.9E-02 | 47 | |
rs405509 | 0.667 | 0.480 | 19 | 44905579 | upstream gene variant | T/G | snv | 0.58 | 30 | ||
rs11542041 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 23 | ||
rs769449 | 0.882 | 0.120 | 19 | 44906745 | non coding transcript exon variant | G/A | snv | 8.4E-02 | 11 | ||
rs440446 | 0.807 | 0.200 | 19 | 44905910 | missense variant | C/G;T | snv | 0.60 | 8 | ||
rs769446 | 0.882 | 0.120 | 19 | 44905371 | upstream gene variant | T/C | snv | 7.0E-02 | 6 | ||
rs769450 | 0.925 | 0.120 | 19 | 44907187 | non coding transcript exon variant | G/A | snv | 0.39 | 5 | ||
rs1233347077 | 0.851 | 0.160 | 19 | 44905894 | missense variant | G/C | snv | 7.0E-06 | 4 | ||
rs199768005 | 0.882 | 0.160 | 19 | 44909057 | missense variant | T/A | snv | 4.5E-04 | 4.9E-04 | 4 | |
rs752600356 | 0.851 | 0.280 | 19 | 44908681 | missense variant | G/A;C | snv | 2.3E-05 | 1.4E-05 | 4 | |
rs761592007 | 0.882 | 0.160 | 19 | 44909013 | missense variant | G/A | snv | 1.5E-05 | 4 | ||
rs748703149 | 0.882 | 0.080 | 19 | 44908729 | missense variant | G/A;C;T | snv | 6.3E-06; 6.3E-06 | 3 | ||
rs449647 | 0.925 | 0.120 | 19 | 44905307 | upstream gene variant | A/T | snv | 0.21 | 2 | ||
rs7259620 | 0.925 | 0.120 | 19 | 44904531 | upstream gene variant | G/A;C | snv | 2 | |||
rs769452 | 0.925 | 0.160 | 19 | 44907853 | missense variant | T/C | snv | 2.5E-03 | 1.9E-03 | 2 | |
rs1081105 | 1.000 | 0.080 | 19 | 44909698 | non coding transcript exon variant | A/C | snv | 3.0E-02 | 1 | ||
rs1167428194 | 1.000 | 0.080 | 19 | 44908634 | missense variant | A/C | snv | 1 | |||
rs1270059098 | 1.000 | 0.080 | 19 | 44906634 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
rs1424027593 | 1.000 | 0.080 | 19 | 44908639 | missense variant | C/A | snv | 1 | |||
rs1438607869 | 1.000 | 0.080 | 19 | 44908741 | missense variant | G/A | snv | 1 | |||
rs1440976751 | 1.000 | 0.080 | 19 | 44907789 | missense variant | G/A | snv | 1 | |||
rs533904656 | 1.000 | 0.080 | 19 | 44907768 | missense variant | G/A;C | snv | 1.8E-04; 8.2E-06 | 1 | ||
rs759721023 | 1.000 | 0.080 | 19 | 44908936 | missense variant | G/A | snv | 8.4E-05 | 6.3E-05 | 1 | |
rs981058595 | 1.000 | 0.080 | 19 | 44908847 | missense variant | C/A | snv | 1 |