{{Rsnum
|rsid=121908540
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC19A2
|position=169485615
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP6V0CP1,SLC19A2
}}{{omim
|id=603941
|rsnum=121908540
|variant=0010
}}{{ClinVar
|rsid=121908540
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=169485615
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=SLC19A2:10560
|GENE_NAME=SLC19A2
|GENE_ID=10560
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.169485615G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006996.2:c.152C>T; 603941.0010
|CLNSIG=5
|CLNCUI=C0342287
|CLNDBN=Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
|Disease=Megaloblastic anemia
|CLNACC=RCV000006328.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1282:C0342287:249270:ORPHA49827:237617006
}}