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: rs1555337681
rs1555337681
1 1.000 14 64424882 missense variant C/T snv 0.800 1.000 3 2011 2017