Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs370244148
rs370244148
Entrez Id: 7482
Gene Symbol: WNT2B
WNT2B
CUI: C1867873
Disease:
Failure to thrive in infancy
T 0.700 CausalMutation CLINVAR