Variant (rsID / SNP)

rs9811771

rs9811771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCD2. Location: chromosome 3, position 10,133,949. Clinical significance in the table: Benign.

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Reference-table entries

FANCD2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:10133949
Cytoband: 3p25.3
HGVS: NM_001018115.3(FANCD2):c.3849+13A>G
Allele change: Silent

Associated conditions / phenotypes

Fanconi anemia complementation group D2|Fanconi anemia|Hereditary breast ovarian cancer syndrome

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.