{{Rsnum
|rsid=386833514
|Chromosome=2
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FSHR
|position=48982918
|Gene_s=FSHR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=2
|CLNACC=RCV000049442.1
|CLNALLE=1
|CLNDBN=Ovarian dysgenesis 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074196:233300:243
|CLNHGVS=NC_000002.11:g.49210057A>C
|CLNSIG=4
|Disease=Ovarian dysgenesis 1
|FwdALT=G
|FwdREF=T
|REF=A
|RSPOS=49210057
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833514
|GENEINFO=FSHR:2492
|GENE_ID=2492
|GENE_NAME=FSHR
}}{{PMID Auto
|PMID=19172541
|Title=A novel mutation in exon8 of the follicle-stimulating hormone receptor in a woman with primary amenorrhea.
}}