{{Rsnum
|rsid=121912539
|Gene=LHCGR
|Chromosome=2
|position=48723650
|Orientation=minus
|GMAF=0.0004591
|Gene_s=LHCGR,STON1-GTF2A1L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{omim
|id=152790
|rsnum=121912539
|variant=0028
}}{{ClinVar
|rsid=121912539
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=48950789
|CHROM=2
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|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.48950789C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=152790.0028
|CLNSIG=5
|CLNCUI=C0266432
|CLNDBN=Leydig cell agenesis
|Disease=Leydig cell agenesis
|CLNACC=RCV000015492.24
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0266432:238320:56212008
|COMMON=0
}}