Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2526358 17 59865224 intron variant A/G snv 0.16 3
rs1292053 1.000 0.040 17 59886176 missense variant A/G snv 0.45 0.46 2
rs201184664 17 59873258 intron variant -/GT delins 2
rs1292048 17 59877710 intron variant A/G snv 0.46 2
rs4047777 17 59882526 intron variant A/T snv 0.27 1
rs1292056 17 59881686 intron variant C/G;T snv 1
rs1292058 17 59880621 intron variant A/C;T snv 1