{{Rsnum
|rsid=386833515
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=FSHR
|position=48968881
|Gene_s=FSHR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=2
|CLNACC=RCV000049443.1
|CLNALLE=1
|CLNDBN=Ovarian dysgenesis 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074196:233300:243
|CLNHGVS=NC_000002.11:g.49196020T>A
|CLNSIG=4
|Disease=Ovarian dysgenesis 1
|FwdALT=T
|FwdREF=A
|REF=T
|RSPOS=49196020
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833515
|GENEINFO=FSHR:2492
|GENE_ID=2492
|GENE_NAME=FSHR
}}{{PMID Auto
|PMID=10551778
|Title=New natural inactivating mutations of the follicle-stimulating hormone receptor: correlations between receptor function and phenotype.
}}