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Variant (rsID / SNP)

rs141074983

WNT10A

rs141074983 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNT10A. Location: chromosome 2, position 219,747,106. 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
2:219747106
Cytoband
2q35
HGVS
NM_025216.3(WNT10A):c.337C>T (p.Arg113Cys)
Allele change
Missense_R113C

Associated conditions / phenotypes

Tooth agenesis, selective, 4|Odonto-onycho-dermal dysplasia|Tooth agenesis, selective, 4

Public references

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