Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4648356 | 1.000 | 0.080 | 1 | 2792599 | intron variant | C/A | snv | 0.39 | 3 | ||
rs10411936 | 1.000 | 0.080 | 19 | 16437564 | intron variant | A/G | snv | 0.63 | 2 | ||
rs10500264 | 1.000 | 0.080 | 19 | 33259408 | intergenic variant | G/A | snv | 0.14 | 2 | ||
rs11949767 | 1.000 | 0.080 | 5 | 177313243 | upstream gene variant | A/C;G | snv | 2 | |||
rs2412973 | 1.000 | 0.080 | 22 | 30133642 | intron variant | C/A | snv | 0.54 | 2 | ||
rs3130000 | 1.000 | 0.080 | 6 | 30660305 | non coding transcript exon variant | A/G;T | snv | 2 | |||
rs4075958 | 1.000 | 0.080 | 5 | 177357511 | upstream gene variant | G/A | snv | 0.21 | 2 | ||
rs4713429 | 1.000 | 0.080 | 6 | 31053240 | upstream gene variant | C/G | snv | 0.20 | 2 | ||
rs630923 | 1.000 | 0.080 | 11 | 118883644 | upstream gene variant | C/A | snv | 0.13 | 2 | ||
rs6801957 | 1.000 | 0.080 | 3 | 38725824 | intron variant | T/C | snv | 0.67 | 2 | ||
rs9260489 | 1.000 | 0.080 | 6 | 29952555 | upstream gene variant | T/A;G | snv | 2 | |||
rs9262615 | 1.000 | 0.080 | 6 | 31053384 | upstream gene variant | C/G | snv | 0.21 | 2 | ||
rs9262635 | 1.000 | 0.080 | 6 | 31057702 | intron variant | A/G | snv | 0.22 | 2 | ||
rs9262636 | 1.000 | 0.080 | 6 | 31058071 | intron variant | A/G | snv | 0.22 | 2 | ||
rs10201872 | 1.000 | 0.080 | 2 | 230242009 | intron variant | C/T | snv | 0.13 | 1 | ||
rs10466829 | 1.000 | 0.080 | 12 | 9723495 | intron variant | G/A | snv | 0.55 | 1 | ||
rs10492972 | 1.000 | 0.080 | 1 | 10293054 | intron variant | T/C | snv | 0.32 | 1 | ||
rs10500817 | 1.000 | 0.080 | 11 | 15626589 | intron variant | T/C | snv | 0.12 | 1 | ||
rs1050391 | 1.000 | 0.080 | 6 | 32950080 | non coding transcript exon variant | A/G | snv | 0.93 | 1 | ||
rs1059174 | 1.000 | 0.080 | 6 | 29726650 | non coding transcript exon variant | C/A;T | snv | 1 | |||
rs10735781 | 1.000 | 0.080 | 1 | 92655550 | intron variant | G/C | snv | 0.57 | 1 | ||
rs10823051 | 1.000 | 0.080 | 10 | 67504839 | intron variant | G/C | snv | 0.13 | 1 | ||
rs10866713 | 1.000 | 0.080 | 5 | 159491886 | intron variant | G/A | snv | 0.16 | 1 | ||
rs11129295 | 1.000 | 0.080 | 3 | 27747289 | intergenic variant | C/T | snv | 0.39 | 1 | ||
rs11539216 | 1.000 | 0.080 | 6 | 32950203 | non coding transcript exon variant | G/A | snv | 3.9E-02 | 1 |