Variant (rsID / SNP)

rs5030878

rs5030878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FPR1. Location: chromosome 19, position 52,250,216. Clinical significance in the table: Benign.

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Reference-table entries

FPR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:52250216
Cytoband: 19q13.41
HGVS: NM_002029.4(FPR1):c.32T>C (p.Ile11Thr)
Allele change: Missense_I11T

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.