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Variant (rsID / SNP)

rs11780

PABPC1L

rs11780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PABPC1L. Location: chromosome 20, position 43,566,787. The table records no clinical significance for this variant.

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Reference-table entries

PABPC1LNot classified
Variant type
synonymous_variant
Chromosome / position
20:43566787
HGVS
NM_001372179.1,c.1746A>G,p.Ser582Ser
Allele change
Synonymous_S577S

Public references

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