RNF168, ring finger protein 168, 165918

N. diseases: 64; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12490312
rs12490312
Entrez Id: 165918;105374307
Gene Symbol: RNF168;LOC105374307
RNF168;LOC105374307
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9865337
rs9865337
Entrez Id: 165918;105374307
Gene Symbol: RNF168;LOC105374307
RNF168;LOC105374307
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs201915239
rs201915239
Entrez Id: 165918
Gene Symbol: RNF168
RNF168
CUI: C2677792
Disease:
Riddle Syndrome 		A 0.700 CausalMutation CLINVAR