Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1051740
rs1051740
56 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
dbSNP: rs17028834
rs17028834
1 4 99311443 intron variant T/C snv 3.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs1979277
rs1979277
45 0.620 0.560 17 18328782 missense variant G/A snv 0.27 0.31 0.010 < 0.001 1 2014 2014
dbSNP: rs2234922
rs2234922
42 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2011 2011
dbSNP: rs4342445
rs4342445
1 6 159677190 3 prime UTR variant G/A snv 0.22 0.010 1.000 1 2011 2011
dbSNP: rs5746134
rs5746134
1 6 159682083 3 prime UTR variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs6983267
rs6983267
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.010 1.000 1 2008 2008