{{Rsnum
|rsid=80358222
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC16A1
|position=112917796
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC16A1
}}{{omim
|id=600682
|rsnum=80358222
|variant=0001
}}{{ClinVar
|rsid=80358222
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=112917796
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=SLC16A1:6566
|GENE_NAME=SLC16A1
|GENE_ID=6566
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.112917796T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_003051.3:c.610A>G; 600682.0001
|CLNSIG=5
|CLNCUI=C1855577
|CLNDBN=Erythrocyte lactate transporter defect
|Disease=Erythrocyte lactate transporter defect
|CLNACC=RCV000009469.2
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1855577:245340
}}