Variant (rsID / SNP)

rs140417066

rs140417066 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFB9. Location: chromosome 8, position 125,555,335. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NDUFB9Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 8:125555335
Cytoband: 8q24.13
HGVS: NM_005005.3(NDUFB9):c.109T>C (p.Tyr37His)
Allele change: Silent

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.