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: rs373950030
rs373950030
3 0.882 0.080 19 7744967 missense variant C/T snv 2.0E-05 2.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs4804803
rs4804803
15 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 0.010 1.000 1 2014 2014