Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1346131223 1.000 6 43777657 missense variant A/G snv 7.4E-06 1
rs749491856 1.000 6 43782071 missense variant A/C snv 1
rs1229919945 1.000 0.040 6 43782041 missense variant T/C snv 1
rs2146323 0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs833070 0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 8
rs3024994 0.776 0.120 6 43775770 non coding transcript exon variant C/T snv 3.8E-02 8
rs3025033 0.807 0.360 6 43783338 non coding transcript exon variant A/G snv 0.18 6
rs833069 0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs833068 0.851 0.120 6 43774790 non coding transcript exon variant G/A snv 0.36 4
rs3025035 0.851 0.240 6 43783622 non coding transcript exon variant C/T snv 0.14 4
rs3025030 0.882 0.200 6 43782850 non coding transcript exon variant G/C snv 0.13 3
rs3025020 0.882 0.240 6 43781373 non coding transcript exon variant C/T snv 0.24 3
rs3025021 0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70 3
rs3024997 0.882 0.120 6 43777370 non coding transcript exon variant G/A snv 0.31 3
rs3025036 1.000 0.080 6 43783932 non coding transcript exon variant G/A;C;T snv 1
rs735286 6 43776884 non coding transcript exon variant C/T snv 0.23 1
rs3025010 6 43779840 non coding transcript exon variant T/C;G snv 1
rs3025000 1.000 0.120 6 43778432 non coding transcript exon variant C/T snv 0.29 0.23 1
rs25648 0.742 0.320 6 43771240 synonymous variant C/G;T snv 8.5E-06; 0.16 11
rs1305315912 1.000 0.080 6 43770736 synonymous variant C/T snv 2
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs3025040 0.882 0.120 6 43785314 3 prime UTR variant C/T snv 0.15 3
rs3025053 0.925 0.120 6 43785588 3 prime UTR variant G/A snv 8.6E-02 2