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: rs10498635
rs10498635
3 0.925 0.080 14 92636964 intron variant C/T snv 0.14 0.810 1.000 3 2010 2015
dbSNP: rs754388
rs754388
7 0.882 0.120 14 92649065 intron variant G/C;T snv 0.010 1.000 1 2014 2014