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: rs2277382
rs2277382
1 1.000 0.040 12 51912437 missense variant C/T snv 8.4E-02 7.7E-02 0.010 1.000 1 2012 2012