{{Rsnum
|rsid = 28928870
|Gene = FSHR
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=2
|position=48963475
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FSHR
}}{{omim
|desc=OVARIAN HYPERSTIMULATION SYNDROME
|id=136435
|rsnum=28928870
|variant=0008
}}
{{ neighbor
| rsid = 28928871
| distance = 353
}}
{{ neighbor
| rsid = 6165
| distance = 427
}}

{{ClinVar
|rsid=28928870
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=49190614
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=FSHR:2492
|GENE_NAME=FSHR
|GENE_ID=2492
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.49190614G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=136435.0008
|CLNSIG=5
|CLNCUI=C0085083
|CLNDBN=Ovarian hyperstimulation syndrome
|Disease=Ovarian hyperstimulation syndrome
|CLNACC=RCV000017637.26
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0085083:608115:129635004
}}

{{PMID Auto
|PMID=18159088
|Title=Association of FSH receptor and CYP19A1 gene variations with sterility and ovarian hyperstimulation syndrome.
}}

{{PMID Auto
|PMID=22401810
|Title=Assessment of FSHR variants and antimullerian hormone in infertility patients with a reduced ovarian response to gonadotropin stimulation.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}