Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2235543 0.925 0.080 1 209687323 intron variant T/A;C snv 4