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Items: 7

VariationLocationGene(s)Condition(s)Clinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:219755054
GRCh38:
Chr2:218890332
WNT10AInborn genetic diseasesUncertain significance
(May 5, 2016)
criteria provided, single submitter
2.
GRCh37:
Chr2:219757580
GRCh38:
Chr2:218892858
WNT10AOdontoonychodermal dysplasia, Schopf-Schulz-Passarge syndrome, Selective tooth agenesis,
Inborn genetic diseases
Uncertain significance
(Apr 12, 2017)
criteria provided, multiple submitters, no conflicts
3.
GRCh37:
Chr2:219745744
GRCh38:
Chr2:218881022
WNT10AOdontoonychodermal dysplasiaPathogenic
(Jul 1, 2009)
no assertion criteria provided
4.
GRCh37:
Chr2:219757867
GRCh38:
Chr2:218893145
WNT10AOdontoonychodermal dysplasiaPathogenic
(Jul 1, 2009)
no assertion criteria provided
5.
GRCh37:
Chr2:219754712
GRCh38:
Chr2:218889990
WNT10AOdontoonychodermal dysplasia, Tooth agenesis, selective, 4, not provided
Pathogenic
(May 1, 2012)
no assertion criteria provided
6.
GRCh37:
Chr2:219755011
GRCh38:
Chr2:218890289
WNT10AOdontoonychodermal dysplasia, Schopf-Schulz-Passarge syndrome, Tooth agenesis, selective, 4,
not specified, not provided, Selective tooth agenesis,
Inborn genetic diseases
Conflicting interpretations of pathogenicity
(Aug 17, 2017)
criteria provided, conflicting interpretations
7.
GRCh37:
Chr2:219747090
GRCh38:
Chr2:218882368
WNT10AOdontoonychodermal dysplasia, Schopf-Schulz-Passarge syndrome, Tooth agenesis, selective, 4,
not provided, Inborn genetic diseases
Pathogenic
(Dec 29, 2017)
criteria provided, multiple submitters, no conflicts
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