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: rs2072592
rs2072592
2 0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 0.010 1.000 1 2010 2010
dbSNP: rs2162679
rs2162679
6 0.851 0.240 12 102477481 intron variant C/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs6218
rs6218
13 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 0.010 1.000 1 2010 2010
dbSNP: rs7956547
rs7956547
2 0.925 0.120 12 102465038 intron variant T/C snv 0.25 0.010 1.000 1 2010 2010
dbSNP: rs978458
rs978458
2 0.925 0.120 12 102408461 intron variant T/C snv 0.69 0.010 1.000 1 2010 2010