RHAG, Rh associated glycoprotein, 6005

N. diseases: 41; N. variants: 13
Disease: Rh-Null, Regulator Type ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918589
rs121918589
Entrez Id: 6005
Gene Symbol: RHAG
RHAG
CUI: C1849387
Disease:
Rh-Null, Regulator Type 		0.800 GeneticVariation UNIPROT Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene. 10467273 1999
dbSNP: rs121918589
rs121918589
Entrez Id: 6005
Gene Symbol: RHAG
RHAG
CUI: C1849387
Disease:
Rh-Null, Regulator Type 		0.800 GeneticVariation UNIPROT Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment. 9716608 1998
dbSNP: rs121918589
rs121918589
Entrez Id: 6005
Gene Symbol: RHAG
RHAG
CUI: C1849387
Disease:
Rh-Null, Regulator Type 		0.800 GeneticVariation UNIPROT A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type. 9454778 1998
dbSNP: rs121918589
rs121918589
Entrez Id: 6005
Gene Symbol: RHAG
RHAG
CUI: C1849387
Disease:
Rh-Null, Regulator Type 		0.800 GeneticVariation UNIPROT Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency. 8563755 1996
dbSNP: rs121918589
rs121918589
Entrez Id: 6005
Gene Symbol: RHAG
RHAG
CUI: C1849387
Disease:
Rh-Null, Regulator Type 		A 0.800 CausalMutation CLINVAR