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: rs6336
rs6336
5 0.827 0.120 1 156879126 missense variant C/T snv 4.2E-02 3.7E-02 0.010 1.000 1 2009 2009