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: rs6355
rs6355
2 0.925 0.080 17 30221792 missense variant C/G snv 1.2E-02 1.2E-02 0.010 1.000 1 2011 2011