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: rs12467476
rs12467476
5 0.925 0.120 2 27602848 intron variant T/C snv 0.23 0.700 1.000 2 2011 2013
dbSNP: rs12478841
rs12478841
5 0.925 0.120 2 27588855 intron variant A/G snv 0.27 0.700 1.000 2 2011 2013
dbSNP: rs13022873
rs13022873
7 0.882 0.120 2 27592643 intron variant A/C;T snv 0.700 1.000 2 2011 2013
dbSNP: rs2068834
rs2068834
10 0.925 0.120 2 27616672 intron variant T/C snv 0.28 0.700 1.000 2 2011 2013
dbSNP: rs2384656
rs2384656
5 0.925 0.120 2 27609188 intron variant A/G snv 0.27 0.700 1.000 2 2011 2013
dbSNP: rs4666000
rs4666000
5 0.925 0.120 2 27616502 intron variant T/C snv 0.28 0.700 1.000 2 2011 2013
dbSNP: rs6760250
rs6760250
5 0.925 0.120 2 27589385 intron variant G/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs4666002
rs4666002
6 0.925 0.120 2 27617773 intron variant G/A;C snv 0.700 1.000 1 2013 2013