Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26