Gene: FAM161A ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 CausalMutation disease CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709 2019
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 GeneticVariation disease CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709 2019
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 CausalMutation disease CLINVAR Diverse clinical phenotypes associated with a nonsense mutation in FAM161A. 26113502 2015
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 CausalMutation disease CLINVAR The efficacy of microarray screening for autosomal recessive retinitis pigmentosa in routine clinical practice. 25999674 2015
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 CausalMutation disease CLINVAR A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa. 26574802 2015
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 CausalMutation disease CLINVAR Dependable and efficient clinical utility of target capture-based deep sequencing in molecular diagnosis of retinitis pigmentosa. 25097241 2014
Entrez Id: 84140
Gene Symbol: FAM161A
FAM161A 		0.500 CausalMutation disease CLINVAR Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa. 20705278 2010