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Variant (rsID / SNP)

rs201215734

FANCF

rs201215734 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCF. Location: chromosome 11, position 22,646,892. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FANCFConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:22646892
Cytoband
11p14.3
HGVS
NM_022725.4(FANCF):c.465A>T (p.Pro155=)
Allele change
Synonymous_P155P

Associated conditions / phenotypes

Fanconi anemia|Fanconi anemia complementation group F

Public references

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