{{Rsnum
|rsid=121912527
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LHCGR
|position=48723689
|Gene_s=LHCGR,STON1-GTF2A1L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=152790
|rsnum=121912527
|variant=0012
}}{{ClinVar
|rsid=121912527
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=48950828
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=STON1-GTF2A1L:286749; LHCGR:3973
|GENE_NAME=STON1-GTF2A1L; LHCGR
|GENE_ID=286749; 3973
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.48950828A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000015475.24
|CLNDBN=Leydig cell hypoplasia, partial
|CLNDSDB=MedGen
|CLNDSDBID=C2673495
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=152790.0012
|Disease=Leydig cell hypoplasia
}}