Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs3448 0.776 0.240 3 49359318 3 prime UTR variant T/C snv 0.76 8
rs10432782 0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs17650792 0.827 0.080 3 49352817 downstream gene variant A/G snv 0.42 6