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: rs386833682
rs386833682
AMT
1 1.000 0.120 3 49420248 missense variant T/A;C snv 4.0E-06; 8.0E-06 0.800 1.000 8 1994 2017