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Items: 2

VariationLocationGene(s)Condition(s)FrequencyClinical significance
(Last reviewed)
Review status
1.
GRCh37:
Chr6:10402823
GRCh38:
Chr6:10402590
TFAP2ABranchiooculofacial syndromePathogenic
(May 1, 2008)
no assertion criteria provided
2.
GRCh37:
Chr6:10404742
GRCh38:
Chr6:10404509
TFAP2ABranchiooculofacial syndromePathogenic
(Apr 1, 2010)
criteria provided, single submitter