Variant (rsID / SNP)

rs10835638

rs10835638 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FSHB. Location: chromosome 11, position 30,252,352. Clinical significance in the table: association.

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Reference-table entries

FSHBAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 11:30252352
Cytoband: 11p14.1
HGVS: NM_000510.2(FSHB):c.-280G>T

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.