Variant (rsID / SNP)
rs41295899
rs41295899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TFR2. Location: chromosome 7, position 100,225,871. Clinical significance in the table: Benign.
Reference-table entries
TFR2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:100225871
- Cytoband
- 7q22.1
- HGVS
- NM_003227.4(TFR2):c.1449C>T (p.Ser483=)
- Allele change
- Synonymous_S483S
Associated conditions / phenotypes
Hereditary hemochromatosis|Hemochromatosis type 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.