Variant (rsID / SNP)

rs9851180

rs9851180 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARP9. Location: chromosome 3, position 122,259,606. The table records no clinical significance for this variant.

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Reference-table entries

PARP9Not classified

Variant type: missense_variant
Chromosome / position: 3:122259606
HGVS: NM_001146102.2,c.1583A>G,p.Tyr528Cys
Allele change: Missense_Y493C

Associated conditions / phenotypes

Missense_Y493C

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.