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: rs773287275
rs773287275
1 1.000 0.080 11 74457515 missense variant C/T snv 4.8E-05 2.1E-05 0.010 1.000 1 2008 2008