Variant (rsID / SNP)

rs61735303

rs61735303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FZD4. Location: chromosome 11, position 86,663,296. 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: 11:86663296
Cytoband: 11q14.2
HGVS: NM_012193.4(FZD4):c.502C>T (p.Pro168Ser)
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.