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Variant (rsID / SNP)

rs4345897

PYROXD2

rs4345897 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PYROXD2. Location: chromosome 10, position 100,147,060. The table records no clinical significance for this variant.

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Reference-table entries

PYROXD2Not classified
Variant type
synonymous_variant
Chromosome / position
10:100147060
HGVS
NM_032709.3,c.1452T>C,p.Phe484Phe
Allele change
Synonymous_F484F

Public references

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