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Variant (rsID / SNP)

rs113513063

POLDIP3

rs113513063 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POLDIP3. Location: chromosome 22, position 42,998,902. The table records no clinical significance for this variant.

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Reference-table entries

POLDIP3Not classified
Variant type
synonymous_variant
Chromosome / position
22:42998902
HGVS
NM_001278657.2,c.324C>A,p.Pro108Pro
Allele change
Synonymous_P108P

Public references

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