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: rs2187668
rs2187668
20 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 0.800 1.000 2 2007 2010
dbSNP: rs12722039
rs12722039
2 0.925 0.120 6 32637507 missense variant G/A snv 5.7E-02 8.4E-02 0.010 1.000 1 1998 1998