Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2523608 0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19 5
rs9260489 1.000 0.080 6 29952555 upstream gene variant T/A;G snv 2
rs2596466 1.000 0.120 6 31437840 intron variant T/C snv 5.3E-02 1
rs9264638 6 31270541 intron variant G/A;C snv 1
rs16899524 6 31394533 non coding transcript exon variant C/T snv 0.10 1
rs2023472 6 30108087 missense variant A/C;G snv 4.1E-06; 0.68 1