"GeneDx"[submitter] AND "NOD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1233093	NM_006092.4(NOD1):c.1722G>A (p.Ala574=)	NOD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1235615	NM_006092.4(NOD1):c.796G>A (p.Glu266Lys)	NOD1 (E266K)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 253643	GRCh37/hg19 7p15.3-14.3(chr7:22935369-32621975)x1	ADCYAP1R1, AQP1 +68 more	Copy number loss	See cases	GPathogenic

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