{{Rsnum
|rsid=386833510
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FSHR
|position=48963778
|Gene_s=FSHR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=2
|CLNACC=RCV000049439.1
|CLNALLE=1
|CLNDBN=Ovarian dysgenesis 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074196:233300:243
|CLNHGVS=NC_000002.11:g.49190917G>C
|CLNSIG=4
|Disease=Ovarian dysgenesis 1
|FwdALT=G
|FwdREF=C
|REF=G
|RSPOS=49190917
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833510
|GENEINFO=FSHR:2492
|GENE_ID=2492
|GENE_NAME=FSHR
}}{{PMID Auto
|PMID=12571157
|Title=A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics.
}}