Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142343894
rs142343894
Entrez Id: 64388
Gene Symbol: GREM2
GREM2
CUI: C4310638
Disease:
TOOTH AGENESIS, SELECTIVE, 9
0.700 GeneticVariation UNIPROT GREMLIN 2 Mutations and Dental Anomalies. 26416033 2015