Variant (rsID / SNP)
rs45557033
rs45557033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCM. Location: chromosome 14, position 45,665,661. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
FANCMBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:45665661
- Cytoband
- 14q21.2
- HGVS
- NM_020937.4(FANCM):c.5627A>G (p.Asn1876Ser)
- Allele change
- Missense_N1850S
Associated conditions / phenotypes
Fanconi anemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.