{{Rsnum
|rsid=121909659
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FSHR
|position=48989022
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FSHR
}}{{omim
|id=136435
|rsnum=121909659
|variant=0003
}}{{ClinVar
|rsid=121909659
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=49216161
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FSHR:2492
|GENE_NAME=FSHR
|GENE_ID=2492
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.49216161A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=136435.0003
|CLNSIG=5
|CLNCUI=CN074196
|CLNDBN=Ovarian dysgenesis 1
|Disease=Ovarian dysgenesis 1
|CLNACC=RCV000017631.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN074196:233300:243
}}