Variant (rsID / SNP)

rs560094

rs560094 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRUNE2. Location: chromosome 9, position 79,318,471. The table records no clinical significance for this variant.

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Reference-table entries

PRUNE2Not classified

Variant type: synonymous_variant
Chromosome / position: 9:79318471
HGVS: NM_015225.3,c.8058G>A,p.Leu2686Leu
Allele change: Synonymous_L2686L

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.