Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10