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: rs121918544
rs121918544
7 0.827 0.200 14 24240635 missense variant C/T snv 0.010 1.000 1 2008 2008