Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1620977
rs1620977
Entrez Id: 257194
Gene Symbol: NEGR1
NEGR1
CUI: C0008074
Disease:
Child Development Disorders, Pervasive
A 0.700 GeneticVariation GWASCAT Identification of common genetic risk variants for autism spectrum disorder. 30804558 2019