SELENBP1, selenium binding protein 1, 8991

N. diseases: 214; N. variants: 8
Disease: EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553204840
rs1553204840
Entrez Id: 8991
Gene Symbol: SELENBP1
SELENBP1
CUI: C4748387
Disease:
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY 		0.800 GeneticVariation UNIPROT Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis. 29255262 2018
dbSNP: rs758495626
rs758495626
Entrez Id: 8991
Gene Symbol: SELENBP1
SELENBP1
CUI: C4748387
Disease:
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY 		0.800 GeneticVariation UNIPROT Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis. 29255262 2018
dbSNP: rs1553204840
rs1553204840
Entrez Id: 8991
Gene Symbol: SELENBP1
SELENBP1
CUI: C4748387
Disease:
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY 		A 0.800 CausalMutation CLINVAR
dbSNP: rs758495626
rs758495626
Entrez Id: 8991
Gene Symbol: SELENBP1
SELENBP1
CUI: C4748387
Disease:
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY 		A 0.800 CausalMutation CLINVAR
dbSNP: rs1357490520
rs1357490520
Entrez Id: 8991
Gene Symbol: SELENBP1
SELENBP1
CUI: C4748387
Disease:
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1553204817
rs1553204817
Entrez Id: 8991
Gene Symbol: SELENBP1
SELENBP1
CUI: C4748387
Disease:
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY 		A 0.700 CausalMutation CLINVAR