Source: ALL
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: rs121909293
rs121909293
CTRC
5 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.010 1.000 1 2011 2011