Gene: CCT5 ×
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: rs118203986
rs118203986
CCT5
2 0.925 0.080 5 10256063 missense variant A/G snv 9.9E-05 3.9E-04 0.010 1.000 1 2017 2017