Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11040869 0.925 0.080 11 1263382 downstream gene variant G/A snv 1.8E-02 2
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 10
rs11084490 0.925 0.080 19 57231104 5 prime UTR variant G/A;C;T snv 0.87; 3.8E-05 2
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs111238176 0.851 0.160 1 172665840 missense variant A/G snv 4
rs11133399 0.925 0.080 4 55547664 non coding transcript exon variant A/G snv 0.28 2
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs111638916 0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs11170877 0.925 0.080 12 54340505 start lost A/G snv 0.16 0.17 2
rs11187842 0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 4
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs112310158 0.925 0.080 5 55170550 non coding transcript exon variant G/A snv 1.7E-03 7.5E-03 2
rs11254413 0.851 0.120 10 17162188 missense variant G/A snv 0.41 0.44 4
rs1126757 0.882 0.120 19 55368504 synonymous variant C/G;T snv 4.1E-06; 0.48 3
rs1126760 0.925 0.080 19 55364706 3 prime UTR variant G/A;C snv 2
rs1126772 0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16 5
rs1127379 0.882 0.120 8 41263761 3 prime UTR variant T/C snv 0.48 3
rs112754928 0.925 0.080 1 31815123 missense variant G/A;T snv 4.5E-03; 1.2E-05 2
rs1127687 0.925 0.080 10 113730350 3 prime UTR variant G/A snv 0.23 2
rs1130233 0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131445 0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs1135354 0.925 0.080 2 102397842 3 prime UTR variant T/G snv 0.23 2
rs113593938 0.790 0.200 21 44250907 missense variant C/T snv 3.5E-03 7