{{Rsnum
|rsid=398122396
|Chromosome=8
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TCCC)
|geno3=(TCCC;TCCC)
|Gene=SLC20A2
|position=42417931
|Gene_s=SLC20A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=8
|CLNACC=RCV000066206.24
|CLNALLE=1
|CLNDBN=Fahr's syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1421:C0393590:213600:1980:110997000
|CLNHGVS=NC_000008.10:g.42275449_42275452delGGGA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=158378.0007
|Disease=Fahr's syndrome
|FwdREF=TCCC
|GENEINFO=SLC20A2:6575
|GENE_ID=6575
|GENE_NAME=SLC20A2
|REF=CGGGA
|RSPOS=42275448
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398122396
}}