Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10004195 | 0.790 | 0.320 | 4 | 38783103 | upstream gene variant | T/A | snv | 0.29 | 8 | ||
rs10022537 | 0.925 | 0.080 | 4 | 16075214 | intron variant | A/T | snv | 0.70 | 2 | ||
rs1002765 | 0.851 | 0.080 | 3 | 87227912 | intron variant | G/A;C | snv | 4 | |||
rs10029005 | 1.000 | 0.080 | 4 | 124530209 | intron variant | G/A | snv | 0.40 | 1 | ||
rs10036748 | 0.752 | 0.360 | 5 | 151078585 | intron variant | C/A;T | snv | 11 | |||
rs10052016 | 0.925 | 0.080 | 5 | 1427996 | intron variant | A/G | snv | 0.22 | 2 | ||
rs10052657 | 0.807 | 0.120 | 5 | 59111944 | intron variant | C/A | snv | 0.17 | 7 | ||
rs10074991 | 0.851 | 0.120 | 5 | 40790449 | intron variant | G/A | snv | 0.31 | 7 | ||
rs10088390 | 0.925 | 0.080 | 8 | 41264249 | 3 prime UTR variant | C/G | snv | 0.19 | 2 | ||
rs1011445550 | 0.925 | 0.080 | 17 | 7676391 | missense variant | G/C | snv | 2 | |||
rs10116253 | 0.851 | 0.120 | 9 | 117702042 | upstream gene variant | T/C | snv | 0.28 | 4 | ||
rs1016343 | 0.807 | 0.240 | 8 | 127081052 | non coding transcript exon variant | C/T | snv | 0.20 | 8 | ||
rs1042028 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 0.22 | 0.30 | 30 | |
rs10421916 | 0.925 | 0.080 | 19 | 17818178 | intron variant | A/G | snv | 0.69 | 2 | ||
rs1042229 | 0.790 | 0.280 | 19 | 51746419 | missense variant | A/C;G | snv | 0.32; 0.13 | 7 | ||
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs1044432 | 0.925 | 0.080 | 11 | 13388251 | 3 prime UTR variant | A/T | snv | 0.16 | 2 | ||
rs1045411 | 0.708 | 0.360 | 13 | 30459095 | 3 prime UTR variant | C/T | snv | 0.20 | 18 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs10464867 | 0.925 | 0.080 | 8 | 89933370 | 3 prime UTR variant | C/T | snv | 3.0E-02 | 2 | ||
rs10474606 | 0.925 | 0.080 | 5 | 80057163 | intron variant | G/A | snv | 0.28 | 2 | ||
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs1047840 | 0.708 | 0.280 | 1 | 241878999 | missense variant | G/A | snv | 0.36 | 0.40 | 19 | |
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 |