NOP10, NOP10 ribonucleoprotein, 55505

N. diseases: 85; N. variants: 1
Disease: Dyskeratosis Congenita ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908092
rs121908092
Entrez Id: 55505;256646
Gene Symbol: NOP10;NUTM1
NOP10;NUTM1
CUI: C0265965
Disease:
Dyskeratosis Congenita 		A 0.700 CausalMutation CLINVAR