Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs7754840 0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 7
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 6
rs9465871 0.882 0.120 6 20717024 intron variant T/C snv 0.30 4
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs4712523 0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs6931514 0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs742642 1.000 0.080 6 20664850 intron variant G/A snv 0.21 3
rs7766070 1.000 0.080 6 20686342 intron variant C/A snv 0.25 3
rs9358356 1.000 0.080 6 20667151 intron variant T/C snv 0.39 3
rs9368219 1.000 0.080 6 20674460 intron variant C/T snv 0.19 3
rs35612982 1.000 0.080 6 20682391 intron variant T/C snv 0.29 2
rs4712524 0.925 0.120 6 20657634 intron variant A/G snv 0.40 2
rs6456368 1.000 0.080 6 20659575 intron variant T/C snv 0.40 2
rs6935599 1.000 0.080 6 20716864 intron variant A/G snv 0.31 2
rs7741604 0.925 0.120 6 20731293 intron variant A/C;T snv 2
rs7747752 1.000 0.080 6 20725192 intron variant G/C snv 0.34 2
rs7767391 1.000 0.080 6 20725009 intron variant T/C snv 0.28 2
rs9348440 1.000 0.080 6 20641105 intron variant C/T snv 0.13 2
rs9350276 1.000 0.080 6 20740065 intron variant C/T snv 0.38 2
rs1040558 1.000 0.080 6 20713475 intron variant A/G snv 0.19 1