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 | 7 | ||
rs10045431 | 0.851 | 0.240 | 5 | 159387525 | intron variant | A/C | snv | 0.78 | 4 | ||
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 | ||
rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
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 | 3 | ||
rs1044165 | 1.000 | 0.080 | X | 66021884 | 3 prime UTR variant | G/A | snv | 9.0E-02 | 1 | ||
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 | 13 | ||
rs104895080 | 0.882 | 0.160 | 16 | 3254380 | missense variant | C/G;T | snv | 6.3E-04 | 3 | ||
rs104895094 | 0.851 | 0.320 | 16 | 3243403 | missense variant | T/A;C | snv | 8.0E-06; 5.2E-03 | 5 | ||
rs104895271 | 0.851 | 0.240 | 12 | 6334161 | missense variant | A/C;G | snv | 1.6E-04; 4.8E-05 | 6 | ||
rs10492503 | 1.000 | 0.080 | 13 | 92232844 | intron variant | T/A | snv | 0.36 | 1 | ||
rs10492972 | 1.000 | 0.080 | 1 | 10293054 | intron variant | T/C | snv | 0.32 | 1 | ||
rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 | |
rs10499194 | 0.752 | 0.400 | 6 | 137681500 | intron variant | C/T | snv | 0.24 | 10 | ||
rs10500264 | 1.000 | 0.080 | 19 | 33259408 | intergenic variant | G/A | snv | 0.14 | 2 | ||
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 | ||
rs10509540 | 0.925 | 0.160 | 10 | 88263276 | upstream gene variant | T/C | snv | 0.25 | 2 | ||
rs1051312 | 0.827 | 0.120 | 20 | 10306440 | 3 prime UTR variant | T/C | snv | 0.20 | 5 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 11 | ||
rs10517086 | 0.882 | 0.160 | 4 | 26083889 | intron variant | G/A | snv | 0.27 | 4 |