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: rs28362459
rs28362459
3 0.925 0.040 19 5844781 missense variant A/C;G;T snv 0.18; 1.2E-05 0.010 1.000 1 2016 2016
dbSNP: rs3745635
rs3745635
3 0.882 0.040 19 5844332 missense variant C/T snv 8.5E-02 0.11 0.010 1.000 1 2016 2016