{{Rsnum
|rsid=121909192
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SMN2
|position=70076545
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SMN2
}}{{omim
|id=601627
|rsnum=121909192
|variant=0001
}}{{ClinVar
|rsid=121909192
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=69372372
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040002110100
|GENEINFO=SMN2:6607
|GENE_NAME=SMN2
|GENE_ID=6607
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.69372372G>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;VLD;OTHERKG;LSD;OM
|CLNACC=RCV000008426.1
|CLNDBN=Spinal muscular atrophy, modifier of
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601627.0001
|Disease=Spinal muscular atrophy
}}