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Variant (rsID / SNP)

rs117132825

ZNF335

rs117132825 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF335. Location: chromosome 20, position 44,588,904. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ZNF335Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
20:44588904
Cytoband
20q13.12
HGVS
NM_022095.4(ZNF335):c.1963C>T (p.Pro655Ser)
Allele change
Missense_P655S

Public references

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