Gene: CWF19L2 ×
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: rs3758911
rs3758911
CWF19L2
1 1.000 0.040 11 107326914 missense variant T/A;C snv 1.3E-05; 0.29 0.700 1.000 1 2018 2018