Variant (rsID / SNP)

rs7800847

rs7800847 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOBOX. Location: chromosome 7, position 144,098,634. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NOBOXBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:144098634
Cytoband: 7q35
HGVS: NM_001080413.3(NOBOX):c.349C>T (p.Arg117Trp)
Allele change: Missense_R117W

Associated conditions / phenotypes

Premature ovarian failure 5|Premature ovarian failure 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.