Variant (rsID / SNP)

rs137854591

rs137854591 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYBB. Clinical significance in the table: Pathogenic.

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Reference-table entries

CYBBPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xp21.1
HGVS: NM_000397.4(CYBB):c.302A>G (p.His101Arg)
Allele change: Missense_H101R

Associated conditions / phenotypes

Granulomatous disease, chronic, X-linked, variant|Granulomatous disease, chronic, X-linked

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.