Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 GeneticVariation phenotype CLINVAR We present a case of TNHP caused by <i>TRPV6</i> gene mutations. 30820485 2019
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 GeneticVariation phenotype UNIPROT We present a case of TNHP caused by <i>TRPV6</i> gene mutations. 30820485 2019
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 GeneticVariation phenotype CLINVAR These results suggest that TNHP is an autosomal-recessive disease caused by TRPV6 mutations that affect maternal-fetal calcium transport. 29861107 2018
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 GeneticVariation phenotype BEFREE These results suggest that TNHP is an autosomal-recessive disease caused by TRPV6 mutations that affect maternal-fetal calcium transport. 29861107 2018
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 Biomarker phenotype GENOMICS_ENGLAND These results suggest that TNHP is an autosomal-recessive disease caused by TRPV6 mutations that affect maternal-fetal calcium transport. 29861107 2018
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 GeneticVariation phenotype UNIPROT These results suggest that TNHP is an autosomal-recessive disease caused by TRPV6 mutations that affect maternal-fetal calcium transport. 29861107 2018
Entrez Id: 55503
Gene Symbol: TRPV6
TRPV6 		0.610 CausalMutation phenotype CLINVAR