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: rs138470268
rs138470268
1 1.000 21 17565541 missense variant C/T snv 4.0E-06 0.010 1.000 1 2014 2014