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: rs1000879
rs1000879
3 2 218439407 intron variant G/A snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs6726798
rs6726798
3 2 218436132 intron variant A/C snv 0.94 0.700 1.000 1 2012 2012