Variant (rsID / SNP)

rs11619791

rs11619791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PABPC3. Location: chromosome 13, position 25,670,984. The table records no clinical significance for this variant.

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Reference-table entries

PABPC3Not classified

Variant type: synonymous_variant
Chromosome / position: 13:25670984
HGVS: NM_030979.3,c.648C>T,p.Pro216Pro
Allele change: Synonymous_P216P

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.