Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174549 0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 8
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 7
rs174566 0.925 0.160 11 61824890 intron variant A/G snv 0.34 7
rs174551 11 61806212 5 prime UTR variant T/C snv 0.28 6
rs174554 1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs174568 1.000 0.080 11 61826344 missense variant C/A;T snv 0.37 3