Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052471595
rs1052471595
NAGLU
A 0.700 CausalMutation CLINVAR Deep sequencing reveals 50 novel genes for recessive cognitive disorders. 21937992

2011
dbSNP: rs1052471595
rs1052471595
NAGLU
A 0.700 GeneticVariation CLINVAR