{{Rsnum
|rsid=61495246
|Gene=CYP2R1
|Chromosome=11
|position=14885847
|Orientation=minus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CYP2R1
}}{{omim
|id=608713
|rsnum=61495246
|variant=0001
}}

{{ClinVar
|rsid=61495246
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=14907393
|CHROM=11
|GMAF=0.0009
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050270000000040016110100
|GENEINFO=CYP2R1:120227
|GENE_NAME=CYP2R1
|GENE_ID=120227
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.14907393A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608713.0001
|CLNSIG=5
|CLNCUI=C1838657
|CLNDBN=Vitamin d hydroxylation-deficient rickets, type 1b
|Disease=Vitamin d hydroxylation-deficient rickets
|CLNACC=RCV000002216.1
|Tags=RV;PM;TPA;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1838657:600081:289157
|COMMON=0
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}