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: rs4377469
rs4377469
CCK
3 3 42261582 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8192472
rs8192472
CCK
3 3 42258378 intron variant C/G;T snv 0.700 1.000 1 2013 2013