Variant (rsID / SNP)
rs150303869
rs150303869 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CP. Location: chromosome 3, position 148,925,398. Clinical significance in the table: Uncertain significance.
Reference-table entries
CPUncertain significance
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:148925398
- Cytoband
- 3q25.1
- HGVS
- NM_000096.4(CP):c.788A>G (p.Asn263Ser)
- Allele change
- Silent
Associated conditions / phenotypes
Deficiency of ferroxidase
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.