Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209970 1.000 0.040 1 41377768 intron variant G/A snv 0.59 2
rs10218712 1 41366625 intron variant T/G snv 0.34 1
rs1892423 1 41383668 downstream gene variant A/C snv 0.49 1
rs2364543 1 41367417 intron variant T/C;G snv 1
rs4636447 1 41369961 intron variant A/G snv 0.63 1
rs56233836 1 41371501 intron variant C/T snv 0.14 1
rs61774743 1 41367189 intron variant C/T snv 0.34 1