{{Rsnum
|rsid=387906652
|Chromosome=8
|position=42417960
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SLC20A2
|Gene_s=SLC20A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,C
|CHROM=8
|CLNACC=RCV000022664.3; RCV000059349.20; RCV000022663.3; RCV000059348.24
|CLNALLE=1; 2
|CLNDBN=Basal ganglia calcification, idiopathic, 3; Fahr's syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1421:C3281142:614540; NBK1421:C0393590:213600:1980:110997000
|CLNHGVS=NC_000008.10:g.42275478G>A; NC_000008.10:g.42275478G>C
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1421; 158378.0003; 158378.0002
|Disease=Basal ganglia calcification; Fahr's syndrome
|FwdALT=G,T
|FwdREF=C
|REF=G
|RSPOS=42275478
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906652
|GENEINFO=SLC20A2:6575
|GENE_ID=6575
|GENE_NAME=SLC20A2
}}