Variant (rsID / SNP)

rs282547

rs282547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARP8. Location: chromosome 5, position 50,057,729. The table records no clinical significance for this variant.

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Reference-table entries

PARP8Not classified

Variant type: synonymous_variant
Chromosome / position: 5:50057729
HGVS: NM_001178055.2,c.420G>A,p.Gly140Gly
Allele change: Synonymous_G140G

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.