{{Rsnum
|rsid=387906654
|Chromosome=8
|position=42428768
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SLC20A2
|Gene_s=SLC20A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000022666.25
|CLNALLE=1
|CLNDBN=Fahr's syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1421:C0393590:213600:1980:110997000
|CLNHGVS=NC_000008.10:g.42286286G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=158378.0005
|Disease=Fahr's syndrome
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=42286286
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906654
|GENEINFO=SLC20A2:6575
|GENE_ID=6575
|GENE_NAME=SLC20A2
}}