Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201167096 1 74534327 intron variant -/T delins 2
rs113313252 1 74534327 intron variant -/T delins 2
rs12142020 1 74534327 intron variant A/T snv 0.50 2
rs1514175 1.000 0.080 1 74525960 intron variant A/G snv 0.48 2