{{Rsnum
|rsid=145191476
|Chromosome=1
|position=108924060
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=GPSM2
|Gene_s=GPSM2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000029165.1
|CLNALLE=1
|CLNDBN=Chudley-McCullough syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858695:604213:ORPHA314597
|CLNHGVS=NC_000001.11:g.108924060C>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_013296.4:c.1661C>A; 609245.0005
|Disease=Chudley-McCullough syndrome
|FwdALT=A
|FwdREF=C
|GENEINFO=GPSM2:29899
|GENE_ID=29899
|GENE_NAME=GPSM2
|REF=C
|RSPOS=108924060
|Reversed=0
|SAO=0
|SSR=0
|Tags=NSN;REF;ASP;OTHERKG
|VC=SNV
|VP=0x050000000605000002000100
|WGT=1
|dbSNPBuildID=134
|rsid=145191476
}}