Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs7953257 12 112246417 intron variant A/G;T snv 0.71 5
rs555346412 12 112191863 intron variant G/C snv 8.2E-04 5
rs11066188 0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 3
rs2285810 12 112261736 non coding transcript exon variant T/C snv 0.45 2
rs4766898 12 112344040 intron variant C/T snv 4.8E-02 1
rs77768175 1.000 0.040 12 112298314 intron variant A/G snv 5.8E-03 1
rs1005902 12 112229871 missense variant T/C;G snv 4.1E-06; 0.42 1
rs11066194 1.000 0.040 12 112212323 intron variant A/G snv 4.8E-02 1
rs2301712 12 112203573 non coding transcript exon variant T/G snv 0.10 9.1E-02 1