Variant (rsID / SNP)

rs35495399

rs35495399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCD2. Location: chromosome 3, position 10,115,033. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FANCD2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:10115033
Cytoband: 3p25.3
HGVS: NM_001018115.3(FANCD2):c.2702G>T (p.Gly901Val)
Allele change: Missense_G901V

Associated conditions / phenotypes

Fanconi anemia|Fanconi anemia complementation group D2|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.