Variant (rsID / SNP)

rs4767884

rs4767884 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PXN. Location: chromosome 12, position 120,661,977. The table records no clinical significance for this variant.

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Reference-table entries

PXNNot classified

Variant type: missense_variant
Chromosome / position: 12:120661977
HGVS: NM_001385981.1,c.217A>G,p.Ser73Gly
Allele change: Missense_S73G

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.