Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9825420 | 0.851 | 0.080 | 3 | 37562521 | intron variant | T/G | snv | 0.18 | 4 | ||
rs10029851 | 0.851 | 0.080 | 4 | 108706869 | intergenic variant | A/C;T | snv | 4 | |||
rs11590421 | 0.851 | 0.080 | 1 | 38528443 | intergenic variant | G/A | snv | 0.15 | 4 | ||
rs1559473 | 0.851 | 0.080 | 2 | 222016799 | intergenic variant | T/G | snv | 0.25 | 4 | ||
rs1605070 | 0.851 | 0.080 | 3 | 51882999 | intergenic variant | C/A | snv | 0.60 | 4 | ||
rs16938145 | 0.851 | 0.080 | 9 | 2256092 | intergenic variant | T/C;G | snv | 4 | |||
rs2322978 | 0.851 | 0.080 | 11 | 127846245 | intergenic variant | A/G | snv | 0.74 | 4 | ||
rs2457174 | 0.851 | 0.080 | 5 | 133843389 | intergenic variant | C/T | snv | 0.33 | 4 | ||
rs2685056 | 0.851 | 0.080 | 3 | 104699729 | intergenic variant | G/A | snv | 0.50 | 4 | ||
rs4424056 | 0.851 | 0.080 | 6 | 91135689 | intergenic variant | T/G | snv | 0.76 | 4 | ||
rs551585 | 0.851 | 0.080 | 1 | 76660688 | intergenic variant | C/A | snv | 8.9E-02 | 4 | ||
rs72911847 | 0.851 | 0.080 | 2 | 193714051 | intergenic variant | A/G | snv | 3.3E-02 | 4 | ||
rs730547 | 0.851 | 0.080 | 17 | 34785087 | intergenic variant | C/T | snv | 0.20 | 4 | ||
rs75285952 | 0.851 | 0.080 | 4 | 27902934 | intergenic variant | G/A | snv | 3.3E-02 | 4 | ||
rs9327881 | 0.851 | 0.080 | 5 | 103389394 | intergenic variant | G/A | snv | 0.13 | 4 | ||
rs9329300 | 0.851 | 0.080 | 10 | 2747402 | intergenic variant | A/C;G | snv | 4 | |||
rs9977018 | 0.851 | 0.080 | 21 | 41616809 | intergenic variant | T/G | snv | 0.24 | 4 | ||
rs11987758 | 0.851 | 0.080 | 8 | 2180583 | regulatory region variant | G/A | snv | 0.12 | 4 | ||
rs4761659 | 0.851 | 0.080 | 12 | 93293308 | regulatory region variant | T/C | snv | 0.89 | 4 | ||
rs121912438 | 0.605 | 0.520 | 21 | 31667299 | missense variant | G/A;C;T | snv | 1.2E-05; 8.0E-06 | 58 | ||
rs74315452 | 0.732 | 0.160 | 21 | 31667356 | missense variant | T/C | snv | 12 | |||
rs80265967 | 0.732 | 0.200 | 21 | 31667290 | missense variant | A/C;T | snv | 1.4E-03 | 1.2E-03 | 16 | |
rs1002442 | 0.851 | 0.080 | 10 | 60043304 | non coding transcript exon variant | T/G | snv | 0.14 | 4 | ||
rs3849942 | 0.776 | 0.200 | 9 | 27543283 | non coding transcript exon variant | T/A;C | snv | 9 | |||
rs3849943 | 0.827 | 0.080 | 9 | 27543384 | non coding transcript exon variant | C/G;T | snv | 5 |