Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56