Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11003123 0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6
rs11089620 1.000 0.080 22 21568167 non coding transcript exon variant C/G snv 0.18 1
rs1110446 0.925 0.120 6 30103160 3 prime UTR variant C/T snv 0.23 2
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs112120857 1.000 0.080 22 39018377 missense variant G/C;T snv 5.2E-05; 5.4E-03 1
rs1126542 1.000 0.080 6 33069647 missense variant T/A;C;G snv 0.24 0.28 1
rs1126769 1.000 0.080 6 33068658 missense variant T/G snv 0.24 0.29 1
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11355458 1.000 0.080 9 125241510 upstream gene variant CC/-;C;CCC;CCCC delins 1
rs1140763 1.000 0.080 9 125235313 3 prime UTR variant G/A;C snv 1
rs114465251 0.925 0.120 6 29830642 intron variant G/A;C snv 2
rs11465817 0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs11466004 1.000 0.080 8 74029040 missense variant C/G;T snv 1.3E-02 1
rs115492845 0.925 0.120 6 30490287 missense variant G/A;T snv 2
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs115494657 0.925 0.120 7 138713456 intron variant G/A snv 5.0E-03 2
rs11568695 1.000 0.080 13 95044286 synonymous variant C/T snv 1.2E-02 4.7E-02 1
rs11569017
EGF
0.925 0.120 4 109980955 missense variant A/T snv 7.3E-02 5.0E-02 2
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11638027 1.000 0.080 15 90302268 intron variant G/T snv 9.9E-02 1
rs11752643 0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02 2
rs11866328 0.925 0.120 16 9768699 intron variant G/T snv 0.38 3
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs12009 1.000 0.080 9 125235024 3 prime UTR variant G/A;T snv 0.54 1