C0018818[trait identifier] AND "Clinical Genetics Research Group, Karo - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 638671	GRCh37/hg19 15q26.3(chr15:100923767-101626187)	LRRK1, ASB7 +3 more	Copy number loss	Esophageal atresia +3 more	GUncertain significance
Select item 638670	Single allele	APBA2, ATP10A +32 more	Complex	Seizure +3 more	GPathogenic
Select item 638672	GRCh37/hg19 22q11.22-11.23(chr22:22971867-23643138)	IGLC1, BCR +5 more	Copy number loss	Ventricular septal defect +2 more	GPathogenic

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