Variant (rsID / SNP)

rs11640794

rs11640794 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF469. Location: chromosome 16, position 88,494,976. Clinical significance in the table: Benign.

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Reference-table entries

ZNF469Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:88494976
Cytoband: 16q24.2
HGVS: NM_001367624.2(ZNF469):c.1098A>C (p.Arg366Ser)
Allele change: Missense_R366S

Associated conditions / phenotypes

Brittle cornea syndrome 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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