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Variant (rsID / SNP)

rs9282680

FANCA

rs9282680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCA. Location: chromosome 16, position 89,805,970. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FANCABenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
16:89805970
Cytoband
16q24.3
HGVS
NM_000135.4(FANCA):c.3935-9G>A
Allele change
Silent

Associated conditions / phenotypes

Fanconi anemia|Fanconi anemia complementation group A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.