Variant (rsID / SNP)

rs11234890

rs11234890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FZD4. Location: chromosome 11, position 86,659,524. Clinical significance in the table: Benign.

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Reference-table entries

FZD4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:86659524
Cytoband: 11q14.2
HGVS: NM_012193.4(FZD4):c.*2660C>T
Allele change: Silent

Associated conditions / phenotypes

Exudative vitreoretinopathy 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.