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: rs1408272
rs1408272
4 6 25842723 intron variant T/G snv 4.0E-02 0.800 1.000 4 2009 2017
dbSNP: rs3887266
rs3887266
6 0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 0.700 1.000 1 2012 2012