{{Rsnum
|rsid=74315375
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC19A2
|position=169468793
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC19A2
}}{{omim
|id=603941
|rsnum=74315375
|variant=0009
}}{{ClinVar
|rsid=74315375
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=169468793
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=SLC19A2:10560
|GENE_NAME=SLC19A2
|GENE_ID=10560
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.169468793C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006996.2:c.1074G>A; 603941.0009
|CLNSIG=5
|CLNCUI=C0342287
|CLNDBN=Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
|Disease=Megaloblastic anemia
|CLNACC=RCV000006327.1
|Tags=RV;PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1282:C0342287:249270:ORPHA49827:237617006
}}