Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs9138 0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs11730582 0.807 0.240 4 87975269 non coding transcript exon variant T/C snv 0.37 10
rs1126616 0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs1126772 0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16 5
rs17524488 0.925 0.040 4 87975555 non coding transcript exon variant -/G delins 4
rs2853744 0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14 4
rs2728127 0.882 0.120 4 87973963 upstream gene variant A/G;T snv 3
rs28357094 0.882 0.160 4 87975645 non coding transcript exon variant T/G snv 0.17 3
rs11728697 0.925 0.080 4 87977789 non coding transcript exon variant C/T snv 0.54 0.46 2
rs11439060 1.000 0.120 4 87975555 non coding transcript exon variant -/G delins 1
rs2853749 0.882 0.160 4 87976662 intron variant C/T snv 0.34 1
rs1370031102 1.000 0.080 4 87982700 missense variant C/T snv 4.0E-06 7.0E-06 1