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Variant (rsID / SNP)

rs1800362

FANCC

rs1800362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCC. Location: chromosome 9, position 97,934,359. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FANCCBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
9:97934359
Cytoband
9q22.32
HGVS
NM_000136.3(FANCC):c.416G>A (p.Gly139Glu)
Allele change
Missense_G139E

Associated conditions / phenotypes

Fanconi anemia|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group A|Fanconi anemia complementation group C|Malignant tumor of breast

Public references

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