{{Rsnum
|rsid=74315508
|Gene=RTN4R
|Chromosome=22
|position=20242778
|Orientation=minus
|GMAF=0.003214
|Gene_s=GNRH1,RTN4R
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{omim
|id=605566
|rsnum=74315508
|variant=0001
}}{{ClinVar
|rsid=74315508
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=20230301
|CHROM=22
|GMAF=0.0032
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=RTN4R:65078
|GENE_NAME=RTN4R
|GENE_ID=65078
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.20230301G>A
|CLNORIGIN=0
|CLNSIG=255
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9968; 0.003214
|CLNACC=RCV000005158.1
|CLNDBN=Schizophrenia, susceptibility to
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605566.0001
|COMMON=1
|Disease=Schizophrenia
}}