{{Rsnum
|rsid=121912525
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=LHCGR
|position=48687950
|Gene_s=LHCGR,STON1-GTF2A1L
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=152790
|rsnum=121912525
|variant=0009
}}{{ClinVar
|rsid=121912525
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=48915089
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|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.48915089G>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000015472.24
|CLNDBN=LEYDIG HYPOPLASIA, TYPE I
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=152790.0009
|Disease=LEYDIG HYPOPLASIA
}}