Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 264
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs1401635 0.925 0.040 11 27672444 intron variant C/G snv 0.73 2