Variant (rsID / SNP)
rs397507559
rs397507559 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCG. Location: chromosome 9, position 35,075,703. The table records no clinical significance for this variant.
Reference-table entries
FANCGNot classified
- Variant type
- Deletion
- Chromosome / position
- 9:35075703
- Cytoband
- 9p13.3
- HGVS
- NM_004629.2(FANCG):c.1183_1192del (p.Glu395fs)
Associated conditions / phenotypes
Fanconi anemia complementation group G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.