Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917893
rs121917893
NLGN3
0.010 GeneticVariation BEFREE Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3. 31119867

2019