LPO, lactoperoxidase, 4025

N. diseases: 32; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555601787
rs1555601787
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C2673873
Disease:
BARDET-BIEDL SYNDROME 13 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs375170572
rs375170572
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C3714506
Disease:
Meckel syndrome type 1 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs375170572
rs375170572
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C4310705
Disease:
JOUBERT SYNDROME 28 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs375170572
rs375170572
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C2673873
Disease:
BARDET-BIEDL SYNDROME 13 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs386834052
rs386834052
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C3714506
Disease:
Meckel syndrome type 1 		G 0.700 CausalMutation CLINVAR
dbSNP: rs730880323
rs730880323
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C3714506
Disease:
Meckel syndrome type 1 		CCCGGG 0.700 CausalMutation CLINVAR