LPO, lactoperoxidase, 4025

N. diseases: 32; N. variants: 12
Disease: BARDET-BIEDL SYNDROME 13 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386834051
rs386834051
Entrez Id: 4025;54903;105371841
Gene Symbol: LPO;MKS1;LOC105371841
LPO;MKS1;LOC105371841
CUI: C2673873
Disease:
BARDET-BIEDL SYNDROME 13 		TCCCGG 0.700 GeneticVariation CLINVAR MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. 16415886 2006