EFNB1, ephrin B1, 1947

N. diseases: 134; N. variants: 19
Disease: Craniofrontonasal dysplasia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556105849
rs1556105849
Entrez Id: 1947
Gene Symbol: EFNB1
EFNB1
CUI: C0220767
Disease:
Craniofrontonasal dysplasia 		C 0.700 GeneticVariation CLINVAR