Variant (rsID / SNP)

rs113910234

rs113910234 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCF. Location: chromosome 11, position 22,646,800. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FANCFBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:22646800
Cytoband: 11p14.3
HGVS: NM_022725.4(FANCF):c.557C>T (p.Ala186Val)
Allele change: Missense_A186V

Associated conditions / phenotypes

Fanconi anemia complementation group F|Fanconi anemia|Malignant tumor of breast

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.