Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 GeneticVariation disease UNIPROT A new human NHERF1 mutation decreases renal phosphate transporter NPT2a expression by a PTH-independent mechanism. 22506049 2012
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 Biomarker disease GENOMICS_ENGLAND NHERF1 mutations and responsiveness of renal parathyroid hormone. 18784102 2008
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 GeneticVariation disease UNIPROT NHERF1 mutations and responsiveness of renal parathyroid hormone. 18784102 2008
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 Biomarker disease GENOMICS_ENGLAND NHERF1 mutations and responsiveness of renal parathyroid hormone. 19073985 2008
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 CausalMutation disease CLINVAR
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 9368
Gene Symbol: SLC9A3R1
SLC9A3R1 		0.700 Biomarker disease CTD_human