{{Rsnum
|rsid=387906986
|Chromosome=1
|position=37537842
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SNIP1
|Gene_s=SNIP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000023695.1
|CLNALLE=1
|CLNDBN=Psychomotor retardation, epilepsy, and craniofacial dysmorphism
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3281055:614501
|CLNHGVS=NC_000001.11:g.37537842T>C
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_024700.3:c.1097A>G; 608241.0001
|Disease=Psychomotor retardation
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=37537842
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387906986
|GENEINFO=SNIP1:79753
|GENE_ID=79753
|GENE_NAME=SNIP1
|CLNORIGIN=1
}}