Variant (rsID / SNP)

rs181894008

rs181894008 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNT5A. Location: chromosome 3, position 55,513,601. Clinical significance in the table: Uncertain significance.

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Reference-table entries

WNT5AUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 3:55513601
Cytoband: 3p14.3
HGVS: NM_003392.7(WNT5A):c.141-9C>T
Allele change: Silent

Associated conditions / phenotypes

Autosomal dominant Robinow 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.