Variant (rsID / SNP)

rs6166

rs6166 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSHR. Location: chromosome 2, position 49,189,921. Clinical significance in the table: Benign.

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Reference-table entries

FSHRBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:49189921
Cytoband: 2p16.3
HGVS: NM_000145.4(FSHR):c.2039G>A (p.Ser680Asn)
Allele change: Missense_S680N

Associated conditions / phenotypes

Ovarian hyperstimulation syndrome|Ovarian dysgenesis 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.