{{Rsnum
|rsid=267606854
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GPSM2
|position=108897592
|Gene_s=GPSM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000001897.1
|CLNALLE=1
|CLNDBN=Chudley-McCullough syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858695:604213:ORPHA314597
|CLNHGVS=NC_000001.11:g.108897592C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_013296.4:c.379C>T; 609245.0001
|Disease=Chudley-McCullough syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=GPSM2:29899
|GENE_ID=29899
|GENE_NAME=GPSM2
|REF=C
|RSPOS=108897592
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000605000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=267606854
|CLNORIGIN=1
}}