Variant (rsID / SNP)

rs137854590

rs137854590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYBB. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CYBBPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xp21.1
HGVS: NM_000397.4(CYBB):c.466G>A (p.Ala156Thr)
Allele change: Missense_A156T

Associated conditions / phenotypes

Granulomatous disease, chronic, X-linked, variant

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.