Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1350033384
rs1350033384
SGSM3
0.010 GeneticVariation BEFREE Functional characterization of a novel FGFR2 mutation, E731K, in craniosynostosis. 21928350

2012