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: rs11170164
rs11170164
6 0.827 0.120 12 52519884 missense variant C/T snv 5.7E-02 5.3E-02 0.010 1.000 1 2009 2009