Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6731
Gene Symbol: SRP72
SRP72 		0.700 Biomarker disease GENOMICS_ENGLAND A landscape of germ line mutations in a cohort of inherited bone marrow failure patients. 29146883 2018
Entrez Id: 6731
Gene Symbol: SRP72
SRP72 		0.700 GeneticVariation disease UNIPROT Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia. 22541560 2012
Entrez Id: 6731
Gene Symbol: SRP72
SRP72 		0.700 GermlineCausalMutation disease ORPHANET Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasia. 22541560 2012
Entrez Id: 6731
Gene Symbol: SRP72
SRP72 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6731
Gene Symbol: SRP72
SRP72 		0.700 CausalMutation disease CLINVAR
Entrez Id: 6731
Gene Symbol: SRP72
SRP72 		0.700 Biomarker disease CTD_human
Entrez Id: 1437
Gene Symbol: CSF2
CSF2 		0.300 Therapeutic disease CTD_human GM-CSF in busulfan overdosage. 2226734 1990
Entrez Id: 375748
Gene Symbol: ERCC6L2
ERCC6L2 		0.300 Biomarker disease CTD_human
Entrez Id: 134218
Gene Symbol: DNAJC21
DNAJC21 		0.300 Biomarker disease CTD_human