Variant (rsID / SNP)

rs186613919

rs186613919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FPR1. Location: chromosome 19, position 52,249,869. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FPR1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:52249869
Cytoband: 19q13.41
HGVS: NM_002029.4(FPR1):c.379G>A (p.Val127Ile)
Allele change: Missense_V127I

Associated conditions / phenotypes

Gingival disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.