"Baylor Genetics"[submitter] AND "MMP21"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1027776	NM_147191.1(MMP21):c.1123C>T (p.Arg375Cys)	MMP21 (R375C)	Single nucleotide variant (missense variant)	Heterotaxy, visceral, 7, autosomal	GUncertain significance
Select item 1027777	NM_147191.1(MMP21):c.890C>T (p.Thr297Met)	MMP21 (T297M)	Single nucleotide variant (missense variant)	Heterotaxy, visceral, 7, autosomal +1 more	GUncertain significance
Select item 625657	GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not provided	GPathogenic

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