NOP56, NOP56 ribonucleoprotein, 10528

N. diseases: 64; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555779353
rs1555779353
Entrez Id: 10528;692213;100302138;105372505
Gene Symbol: NOP56;SNORD110;MIR1292;LOC105372505
NOP56;SNORD110;MIR1292;LOC105372505
CUI: C3472711
Disease:
Spinocerebellar ataxia 36 		AGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCTGGGCCT 0.700 CausalMutation CLINVAR