"Broad Center for Mendelian Genomics, Broad Institute of MIT and Harva - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 986383	NM_001822.7(CHN1):c.80C>G (p.Ala27Gly)	CHN1 (A27G)	Single nucleotide variant (missense variant +2 more)	Duane retraction syndrome 2 +1 more	GUncertain significance
Select item 3061808	NM_001822.7(CHN1):c.62A>G (p.Tyr21Cys)	CHN1 (Y21C)	Single nucleotide variant (missense variant +2 more)	Duane retraction syndrome 2	GUncertain significance