Variant (rsID / SNP)
rs78488639
rs78488639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FPR1. Location: chromosome 19, position 52,249,959. Clinical significance in the table: Benign.
Reference-table entries
FPR1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:52249959
- Cytoband
- 19q13.41
- HGVS
- NM_002029.4(FPR1):c.289C>A (p.Leu97Met)
- Allele change
- Missense_L97M
Associated conditions / phenotypes
Gingival disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.