{{Rsnum
|rsid=121909533
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALDOA
|position=30068824
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALDOA
}}{{omim
|id=103850
|rsnum=121909533
|variant=0001
}}{{ClinVar
|rsid=121909533
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=30080145
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ALDOA:226
|GENE_NAME=ALDOA
|GENE_ID=226
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.30080145A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=103850.0001
|CLNSIG=5
|CLNCUI=C0272066
|CLNDBN=HNSHA due to aldolase A deficiency
|Disease=HNSHA due to aldolase A deficiency
|CLNACC=RCV000019808.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0272066:611881:57:111578003
}}