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Variant (rsID / SNP)

rs11060

PLG

rs11060 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLG. Location: chromosome 6, position 161,173,946. The table records no clinical significance for this variant.

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Reference-table entries

PLGNot classified
Variant type
synonymous_variant
Chromosome / position
6:161173946
HGVS
NM_000301.5,c.2286T>G,p.Gly762Gly
Allele change
Synonymous_G762G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.