Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77641731
ABO
1.000 0.036 9 133257521 missense variant snp 3
rs28670903 15 32640104 intergenic variant G/T snp 1
rs34379766 12 56080359 missense variant C/A,T snp 4.6E-06; 4.6E-06 1
rs6061910 20 61933124 splice region variant G/A snp 1
rs9937036 16 16636871 intergenic variant T/A,C,G snp 1
rs4362633 20 17464490 non coding transcript exon variant A/C snp 0.10 1
rs6931262 6 7217284 non coding transcript exon variant C/T snp 0.10 1
rs12531027 7 15296311 intron variant T/C snp 0.10 1
rs17104363 14 67472766 3 prime UTR variant T/C snp 0.11 1
rs17473118 3 43402042 intron variant G/A,C snp 0.11 1
rs11231693 11 64095140 intron variant G/A snp 0.12 2
rs4749080 10 25873837 intergenic variant A/G snp 0.12 1
rs3027012 1 159204333 5 prime UTR variant C/T snp 0.13 4
rs9312517 4 167218229 intron variant A/G snp 0.13 1
rs3783637 14 54881400 intron variant C/T snp 0.13 1
rs7981515 13 91870760 intron variant G/T snp 0.14 1
rs920016 8 68628983 intron variant A/C snp 0.14 1
rs7328464 13 91849410 intron variant C/T snp 0.14 1
rs4958456 5 150243802 intron variant C/T snp 0.14 1
rs641862 13 110137885 T/C snp 1.4E-02 1
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs12104221 19 3797102 intron variant C/T snp 0.14 1
rs16933006 9 15335916 intergenic variant A/C snp 0.14 1
rs6044834 20 17455828 intron variant T/G snp 0.15 1
rs1913185 3 146170670 intergenic variant T/G snp 0.15 1