{{Rsnum
|rsid=121434451
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HR
|position=22119227
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HR
}}{{omim
|id=602302
|rsnum=121434451
|variant=0012
}}{{ClinVar
|rsid=121434451
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=21976740
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=HR:55806
|GENE_NAME=HR
|GENE_ID=55806
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.21976740C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602302.0012
|CLNSIG=5
|CLNCUI=C1859877
|CLNDBN=Alopecia universalis congenita
|Disease=Alopecia universalis congenita
|CLNACC=RCV000007765.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1859877:203655:701
}}