Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs121908119

WNT10A

rs121908119 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WNT10A. Location: chromosome 2, position 219,747,090. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

WNT10AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:219747090
Cytoband
2q35
HGVS
NM_025216.3(WNT10A):c.321C>A (p.Cys107Ter)
Allele change
Nonsense_C107X

Associated conditions / phenotypes

Odonto-onycho-dermal dysplasia|SchC6pf-Schulz-Passarge syndrome|Tooth agenesis, selective, 4|Inborn genetic diseases|Tooth agenesis, selective, 4|SchC6pf-Schulz-Passarge syndrome|Odonto-onycho-dermal dysplasia|Tooth agenesis, selective, 4|Odonto-onycho-dermal dysplasia|WNT10A-Related Disorders|Ectodermal dysplasia

Public references

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