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: rs37369
rs37369
9 0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 0.700 1.000 1 2011 2011