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: rs62026376
rs62026376
2 0.925 0.120 16 11134855 intron variant C/T snv 0.18 0.710 1.000 1 2014 2014
dbSNP: rs887864
rs887864
2 0.925 0.120 16 11065028 intron variant G/A;C;T snv 0.700 1.000 1 2011 2011