{{Rsnum
|rsid=397515553
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SMS
|position=21992634
|Gene_s=SMS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C,G
|CHROM=X
|CLNACC=RCV000055907.1; RCV000074415.15
|CLNALLE=1; 2
|CLNDBN=Snyder Robinson syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK144284:C0796160:309583:3063
|CLNHGVS=NC_000023.10:g.22010752A>C; NC_000023.10:g.22010752A>G
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK144284; 300105.0004
|Disease=Snyder Robinson syndrome
|FwdALT=C,G
|FwdREF=A
|GENEINFO=SMS:6611
|GENE_ID=6611
|GENE_NAME=SMS
|REF=A
|RSPOS=22010752
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515553
}}