Variant (rsID / SNP)

rs6617041

rs6617041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POF1B. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

POF1BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq21.1
HGVS: NM_024921.4(POF1B):c.*368G>T
Allele change: Silent

Associated conditions / phenotypes

Premature ovarian failure 2B

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.