Variant (rsID / SNP)

rs4390468

rs4390468 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POSTN. Location: chromosome 13, position 38,138,730. The table records no clinical significance for this variant.

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Reference-table entries

POSTNNot classified

Variant type: intron_variant
Chromosome / position: 13:38138730
HGVS: NM_006475.3,c.2432-33G>A
Allele change: Silent

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.