"Baylor Genetics"[submitter] AND "MAP3K7"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031662	NM_145331.3(MAP3K7):c.1356+9A>G	MAP3K7	Single nucleotide variant (intron variant)	Frontometaphyseal dysplasia 2	GUncertain significance
Select item 1031196	NM_145331.3(MAP3K7):c.868-17T>A	MAP3K7	Single nucleotide variant (intron variant)	Cardiospondylocarpofacial syndrome	GUncertain significance