Variant (rsID / SNP)
rs7103
rs7103 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CPOX. Location: chromosome 3, position 98,298,600. Clinical significance in the table: Benign.
Reference-table entries
CPOXBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:98298600
- Cytoband
- 3q11.2
- HGVS
- NM_000097.7(CPOX):c.*927G>A
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary coproporphyria
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.