Variant (rsID / SNP)

rs5998478

rs5998478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BPIFC. Location: chromosome 22, position 32,811,952. The table records no clinical significance for this variant.

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Reference-table entries

BPIFCNot classified

Variant type: missense_variant
Chromosome / position: 22:32811952
HGVS: NM_174932.3,c.1351T>C,p.Ser451Pro
Allele change: Missense_S451P

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.