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Variant (rsID / SNP)

rs190178539

ZNF335

rs190178539 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF335. Location: chromosome 20, position 44,587,908. 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
20:44587908
Cytoband
20q13.12
HGVS
NM_022095.4(ZNF335):c.2185A>T (p.Ile729Phe)
Allele change
Missense_I729F

Public references

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