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Variant (rsID / SNP)

rs188798140

WNT5A

rs188798140 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNT5A. Location: chromosome 3, position 55,513,600. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

WNT5AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:55513600
Cytoband
3p14.3
HGVS
NM_003392.7(WNT5A):c.141-8C>G
Allele change
Silent

Associated conditions / phenotypes

Autosomal dominant Robinow syndrome 1

Public references

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