Variant (rsID / SNP)

rs1499280

rs1499280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PELO, ITGA1. Location: chromosome 5, position 52,096,889. The table records no clinical significance for this variant.

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Reference-table entries

PELONot classified

Variant type: missense_variant
Chromosome / position: 5:52096889
HGVS: NM_015946.5,c.661C>A,p.Leu221Met
Allele change: Missense_L221M

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.