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Variant (rsID / SNP)

rs104894223

FZD4

rs104894223 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FZD4. Location: chromosome 11, position 86,663,032. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FZD4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:86663032
Cytoband
11q14.2
HGVS
NM_012193.4(FZD4):c.766A>G (p.Ile256Val)
Allele change
Silent

Associated conditions / phenotypes

Retinopathy of prematurity|Exudative vitreoretinopathy 1

Public references

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