{{Rsnum
|rsid=267606922
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NRXN1
|position=50496039
|Gene_s=NRXN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=2
|CLNACC=RCV000009608.1
|CLNALLE=1
|CLNDBN=Pitt-Hopkins-like syndrome 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280479:614325:221150
|CLNHGVS=NC_000002.11:g.50723177G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600565.0002
|Disease=Pitt-Hopkins-like syndrome 2
|FwdALT=G
|FwdREF=C
|GENEINFO=NRXN1:9378
|GENE_ID=9378
|GENE_NAME=NRXN1
|REF=G
|RSPOS=50723177
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606922
}}