NRXN1, neurexin 1, 9378

N. diseases: 139; N. variants: 41
Disease: CHROMOSOME 2p16.3 DELETION SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1558507406
rs1558507406
Entrez Id: 9378
Gene Symbol: NRXN1
NRXN1
CUI: C3808494
Disease:
CHROMOSOME 2p16.3 DELETION SYNDROME 		CCCGT 0.700 SusceptibilityMutation CLINVAR