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Variant (rsID / SNP)

rs121909659

FSHR

rs121909659 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSHR. Location: chromosome 2, position 49,216,161. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FSHRConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:49216161
Cytoband
2p16.3
HGVS
NM_000145.4(FSHR):c.479T>C (p.Ile160Thr)
Allele change
Missense_I160T

Associated conditions / phenotypes

Ovarian dysgenesis 1|Ovarian hyperstimulation syndrome

Public references

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