Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs7776054 6 135097778 intron variant A/G snv 0.24 13
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs17758695 18 63253621 intron variant C/T snv 2.1E-02 10
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs9399137 0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs78909033 2 240571486 intron variant G/A snv 9.2E-02 5
rs149290349 2 43224818 missense variant G/A;T snv 6.7E-02 3
rs1555405 14 100710432 regulatory region variant G/A snv 0.29 2