B9D2, B9 domain containing 2, 80776

N. diseases: 66; N. variants: 13
Disease: MECKEL SYNDROME, TYPE 10 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1487082103
rs1487082103
Entrez Id: 7040;80776
Gene Symbol: TGFB1;B9D2
TGFB1;B9D2
CUI: C3280036
Disease:
MECKEL SYNDROME, TYPE 10 		0.700 GeneticVariation UNIPROT