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Items: 5

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr2:219745744
GRCh38:
Chr2:218881022
WNT10AOdontoonychodermal dysplasiaPathogenic
(Jul 1, 2009)
no assertion criteria provided
2.
GRCh37:
Chr2:219757867
GRCh38:
Chr2:218893145
WNT10AOdontoonychodermal dysplasiaPathogenic
(Jul 1, 2009)
no assertion criteria provided
3.
GRCh37:
Chr2:219754712
GRCh38:
Chr2:218889990
WNT10AOdontoonychodermal dysplasia, Tooth agenesis, selective, 4, not provided
GO-ESP:0.00008(A)Pathogenic
(May 1, 2012)
no assertion criteria provided
4.
GRCh37:
Chr2:219755011
GRCh38:
Chr2:218890289
WNT10AOdontoonychodermal dysplasia, Tooth agenesis, selective, 4GO-ESP:0.01854(A)
GMAF:0.00600(A)
Pathogenic
(Feb 1, 2014)
no assertion criteria provided
5.
GRCh37:
Chr2:219747090
GRCh38:
Chr2:218882368
WNT10AOdontoonychodermal dysplasia, Schopf-Schulz-Passarge syndrome, Tooth agenesis, selective, 4,
Inborn genetic diseases
GO-ESP:0.00100(A)Pathogenic
(May 1, 2012)
criteria provided, single submitter
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