BBS2, Bardet-Biedl syndrome 2, 583

N. diseases: 128; N. variants: 60
Disease: Melanocortin 4 Receptor Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039797
rs886039797
Entrez Id: 583
Gene Symbol: BBS2
BBS2
CUI: C4054546
Disease:
Melanocortin 4 Receptor Deficiency 		C 0.700 GeneticVariation CLINVAR