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: rs6486291
rs6486291
2 11 16465347 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs7925853
rs7925853
4 11 16374856 intron variant A/T snv 4.8E-02 0.700 1.000 1 2012 2012