Variant (rsID / SNP)

rs6169

rs6169 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSHB. Location: chromosome 11, position 30,255,185. Clinical significance in the table: Benign.

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Reference-table entries

FSHBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:30255185
Cytoband: 11p14.1
HGVS: NM_001382289.1(FSHB):c.228C>T (p.Tyr76=)
Allele change: Synonymous_Y76Y

Associated conditions / phenotypes

Hypogonadotropic hypogonadism 24 without anosmia

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.