PROM1, prominin 1, 8842

N. diseases: 477; N. variants: 33
Disease: Retinal Dystrophies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853400
rs878853400
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C0854723
Disease:
Retinal Dystrophies 		A 0.700 GeneticVariation CLINVAR