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Variant (rsID / SNP)

rs184894059

ZNF469

rs184894059 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF469. Location: chromosome 16, position 88,497,350. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ZNF469Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:88497350
Cytoband
16q24.2
HGVS
NM_001367624.2(ZNF469):c.3472C>T (p.Pro1158Ser)
Allele change
Missense_P1130S

Associated conditions / phenotypes

Brittle cornea syndrome 1

Public references

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