Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11166389 1.000 0.040 1 100000723 non coding transcript exon variant G/A snv 0.15 2
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs782414948 1.000 0.040 7 102227624 missense variant G/A snv 3.2E-05 2.8E-05 1
rs749124997 1.000 0.040 12 102402539 missense variant C/T snv 4.0E-06 1
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs3212112 1.000 0.040 14 103699345 intron variant A/C snv 7.1E-03 2.2E-02 1
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs11598018 1.000 0.040 10 103901557 intron variant C/A;T snv 2
rs71305152 0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs3851634 0.882 0.040 12 106419124 intron variant T/C snv 0.22 4
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs10494090 1.000 0.040 1 108150714 intron variant A/C;G;T snv 2
rs10131 1.000 0.040 13 108207498 3 prime UTR variant C/T snv 0.12 3
rs1805388 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs3093739 1.000 0.040 13 108215053 intron variant A/G snv 8.8E-02 1
rs3092993 0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs4845964 1.000 0.040 1 10920487 regulatory region variant G/A snv 0.36 2
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs776728511
EGF
0.925 0.040 4 109945192 missense variant A/G snv 4.0E-06 2