Variant (rsID / SNP)

rs104886459

rs104886459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCC. Location: chromosome 9, position 98,011,507. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FANCCPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 9:98011507
Cytoband: 9q22.32
HGVS: NM_000136.3(FANCC):c.67del (p.Asp23fs)

Associated conditions / phenotypes

Fanconi anemia complementation group C|Fanconi anemia|Hereditary cancer-predisposing 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.