Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1004446 | 0.827 | 0.240 | 11 | 2148913 | intron variant | G/A | snv | 0.37 | 1 | ||
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 1 | ||
rs1014486 | 1.000 | 0.080 | 3 | 159973324 | intron variant | T/C | snv | 0.39 | 1 | ||
rs10201872 | 1.000 | 0.080 | 2 | 230242009 | intron variant | C/T | snv | 0.13 | 1 | ||
rs1021156 | 1.000 | 0.080 | 8 | 78663569 | intron variant | T/C | snv | 0.64 | 1 | ||
rs1036207 | 1.000 | 0.080 | 5 | 142119476 | intron variant | A/G;T | snv | 3 | |||
rs10411936 | 1.000 | 0.080 | 19 | 16437564 | intron variant | A/G | snv | 0.63 | 2 | ||
rs10466829 | 1.000 | 0.080 | 12 | 9723495 | intron variant | G/A | snv | 0.55 | 1 | ||
rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 7 | ||
rs10492972 | 1.000 | 0.080 | 1 | 10293054 | intron variant | T/C | snv | 0.32 | 1 | ||
rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 1 | ||
rs10500264 | 1.000 | 0.080 | 19 | 33259408 | intergenic variant | G/A | snv | 0.14 | 1 | ||
rs10509540 | 0.925 | 0.160 | 10 | 88263276 | upstream gene variant | T/C | snv | 0.25 | 1 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 1 | ||
rs10517086 | 0.882 | 0.160 | 4 | 26083889 | intron variant | G/A | snv | 0.27 | 1 | ||
rs1052553 | 0.827 | 0.200 | 17 | 45996523 | synonymous variant | A/G | snv | 0.14 | 0.15 | 1 | |
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 5 | |
rs1064395 | 0.882 | 0.120 | 19 | 19250926 | 3 prime UTR variant | G/A | snv | 0.24 | 1 | ||
rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 3 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 1 | ||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 6 | |||
rs1077667 | 0.925 | 0.120 | 19 | 6668961 | intron variant | C/G;T | snv | 1 | |||
rs10797431 | 0.851 | 0.080 | 1 | 2569783 | non coding transcript exon variant | G/T | snv | 0.42 | 5 | ||
rs10800309 | 0.925 | 0.120 | 1 | 161502368 | upstream gene variant | A/G;T | snv | 2 | |||
rs10806425 | 0.851 | 0.280 | 6 | 90216893 | intron variant | C/A | snv | 0.33 | 2 |