Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17762454 0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs11755724 0.807 0.320 6 7118757 intron variant A/G;T snv 3
rs1285879 0.925 0.120 6 7137130 intron variant T/C snv 0.67 2
rs1285875 0.925 0.120 6 7115694 intron variant G/A;C snv 0.63 2
rs1285874 0.925 0.120 6 7115300 intron variant T/A snv 0.66 2
rs630258 0.925 0.120 6 7134168 intron variant T/C snv 0.67 2
rs665723 0.925 0.120 6 7138831 intron variant C/T snv 0.67 2
rs6933716 0.925 0.120 6 7125476 intron variant T/C snv 0.53 2
rs2842895 0.925 0.120 6 7106083 upstream gene variant G/C snv 0.40 2
rs622404 0.925 0.120 6 7130363 intron variant A/G snv 0.68 2
rs687467 0.925 0.120 6 7127843 intron variant A/G;T snv 2
rs4585612 0.925 0.120 6 7152919 intron variant C/T snv 0.41 2
rs1334577 0.925 0.120 6 7211518 intron variant G/A snv 0.23 2
rs3778321 6 7250037 3 prime UTR variant G/A snv 0.11 2
rs557074 1.000 0.040 6 7144958 intron variant T/G snv 0.27 1
rs6931262 6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs6935691 6 7178306 intron variant T/A snv 0.28 1
rs9406002 6 7181502 non coding transcript exon variant A/G snv 0.25 1
rs9405328 6 7166005 intron variant A/G snv 0.29 1
rs9502560 6 7176907 intron variant T/G snv 0.29 1
rs9505057 6 7171174 intron variant T/G snv 0.30 1
rs2714337 6 7240344 intron variant A/T snv 0.34 1