Variant (rsID / SNP)

rs370510954

rs370510954 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCC. Location: chromosome 9, position 97,887,367. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

FANCCLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:97887367
Cytoband: 9q22.32
HGVS: NM_000136.3(FANCC):c.996+1G>T
Allele change: Silent

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.