Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10036748 | 0.752 | 0.360 | 5 | 151078585 | intron variant | C/A;T | snv | 11 | |||
rs10434 | 0.701 | 0.480 | 6 | 43785475 | 3 prime UTR variant | A/G | snv | 0.59 | 17 | ||
rs10516487 | 0.752 | 0.360 | 4 | 101829919 | missense variant | G/A;T | snv | 0.26; 8.0E-06 | 11 | ||
rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
rs10822050 | 0.724 | 0.240 | 10 | 62679011 | downstream gene variant | T/C | snv | 0.33 | 14 | ||
rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 40 | ||
rs10988542 | 0.724 | 0.240 | 9 | 129894985 | intron variant | G/A;C | snv | 14 | |||
rs11117431 | 0.807 | 0.160 | 16 | 85981710 | intron variant | A/G | snv | 0.18 | 6 | ||
rs11145763 | 0.724 | 0.240 | 9 | 136369144 | intron variant | A/C;G;T | snv | 14 | |||
rs1137100 | 0.627 | 0.640 | 1 | 65570758 | missense variant | A/G | snv | 0.30 | 0.25 | 39 | |
rs114846446 | 0.724 | 0.240 | 2 | 2944140 | intron variant | G/A | snv | 9.5E-03 | 14 | ||
rs11580078 | 0.724 | 0.240 | 1 | 67203951 | intron variant | C/A;G | snv | 14 | |||
rs117372389 | 0.724 | 0.240 | 16 | 50634166 | 3 prime UTR variant | G/T | snv | 1.1E-02 | 14 | ||
rs11741255 | 0.724 | 0.240 | 5 | 132475490 | intron variant | G/A | snv | 0.29 | 14 | ||
rs11839053 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 14 | ||
rs1217414 | 0.882 | 0.120 | 1 | 113870045 | non coding transcript exon variant | G/A | snv | 0.36 | 3 | ||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 18 | ||
rs1250563 | 0.724 | 0.240 | 10 | 79287626 | intron variant | G/C | snv | 0.24 | 14 | ||
rs12598357 | 0.724 | 0.240 | 16 | 28329624 | intergenic variant | A/G | snv | 0.43 | 15 | ||
rs1267499 | 0.807 | 0.160 | 6 | 14715651 | intron variant | T/A;C | snv | 6 | |||
rs12720356 | 0.752 | 0.360 | 19 | 10359299 | missense variant | A/C;G | snv | 6.1E-02; 4.0E-06 | 12 | ||
rs12863738 | 0.724 | 0.240 | X | 136949968 | intron variant | C/T | snv | 0.16 | 14 | ||
rs12928404 | 0.724 | 0.240 | 16 | 28835925 | splice region variant | T/C | snv | 0.44 | 0.45 | 15 |