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Variant (rsID / SNP)

rs577993

PRUNE2

rs577993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRUNE2. Location: chromosome 9, position 79,321,871. The table records no clinical significance for this variant.

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Reference-table entries

PRUNE2Not classified
Variant type
synonymous_variant
Chromosome / position
9:79321871
HGVS
NM_015225.3,c.5319G>A,p.Thr1773Thr
Allele change
Synonymous_T1773T

Public references

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