ClinVar for MedGen (Select 370865) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 16632	NM_001427.4(EN2):c.686-921T>C	EN2	Single nucleotide variant (intron variant)	Autism, susceptibility to, 10	GUncertain significance
Select item 16631	NM_001427.4(EN2):c.686-1073G>A	EN2	Single nucleotide variant (intron variant)	Autism, susceptibility to, 10	GUncertain significance