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Variant (rsID / SNP)

rs146902156

WNT10A

rs146902156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNT10A. Location: chromosome 2, position 219,754,978. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

WNT10AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:219754978
Cytoband
2q35
HGVS
NM_025216.3(WNT10A):c.649G>A (p.Asp217Asn)
Allele change
Missense_D217N

Associated conditions / phenotypes

Tooth agenesis, selective, 4|SchC6pf-Schulz-Passarge syndrome|Odonto-onycho-dermal dysplasia

Public references

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