Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878854417
rs878854417
HECW2
0.800 GeneticVariation UNIPROT De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs878854417
rs878854417
HECW2
A 0.800 CausalMutation CLINVAR