Gene entry
FANCA
FA complementation group A
- Chromosome
- 16
- Cytoband
- 16q24.3
- Variants (rsID)
- 41
FANCA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q24.3). Its official name is “FA complementation group A”. The reference table lists 41 variants (rsID) for this gene.
Clinically classified variants
29 reference-table entries with clinical significance.
- rs1131660Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs11647746Benignsingle nucleotide variant
- rs138417003Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs149531696Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs17233141Benignsingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia
- rs1800337Benignsingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia
- rs1800347Benignsingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia
- rs34159559Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs34592408Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs55758861Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs7195066Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs75501942Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs9282680Benignsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs139235751Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs149112292Conflicting interpretationssingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia
- rs17227403Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs191943709Conflicting interpretationssingle nucleotide variantInborn genetic diseases|Fanconi anemia|Fanconi anemia complementation group A
- rs368376237Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs757500718Conflicting interpretationssingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs886038245Conflicting interpretationssingle nucleotide variantFanconi anemia complementation group A
- rs9282684Conflicting interpretationssingle nucleotide variantFanconi anemia complementation group A|Fanconi anemia
- rs148100796Pathogenicsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs149277003Pathogenicsingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
- rs397507552PathogenicMicrosatelliteFanconi anemia complementation group A|Fanconi anemia
- rs747851434PathogenicDuplicationFanconi anemia complementation group A|Fanconi anemia
- rs756367276PathogenicDuplicationFanconi anemia|Fanconi anemia complementation group A
- rs864622187PathogenicDeletionFanconi anemia|Fanconi anemia complementation group A
- rs864622188PathogenicMicrosatelliteFanconi anemia|Fanconi anemia complementation group A
- rs201323171Uncertain significancesingle nucleotide variantFanconi anemia|Fanconi anemia complementation group A
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.