Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs25648 0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs833070 0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs3024994 0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs1287276985 0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs3025033 0.807 0.360 6 43783338 non coding transcript exon variant A/G snv 0.18 6
rs752907384 0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6
rs1005230 0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs833069 0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs1188254133 0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4
rs1284410244 0.925 0.040 6 43778482 missense variant A/G snv 7.0E-06 4
rs13207351 0.851 0.280 6 43770057 upstream gene variant A/G;T snv 4
rs138551969 1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs3025021 0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 4
rs3025035 0.851 0.240 6 43783622 non coding transcript exon variant C/T snv 0.14 4
rs833068 0.851 0.120 6 43774790 non coding transcript exon variant G/A snv 0.36 4
rs914956206 0.882 0.080 6 43770762 missense variant G/A;T snv 4