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: rs6805251
rs6805251
4 0.925 0.120 3 119841759 intron variant T/A;C snv 0.800 1.000 2 2013 2017
dbSNP: rs16830551
rs16830551
4 3 119834031 intron variant C/T snv 2.4E-02 0.700 1.000 1 2012 2012