ClinVar Miner

List of variants reported as likely benign for Intellectual disability, autosomal recessive 3

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_017721.5(CC2D1A):c.566C>T (p.Ala189Val)	rs61740117	0.00691
NM_017721.5(CC2D1A):c.1399C>G (p.Pro467Ala)	rs199717745	0.00060
NM_017721.5(CC2D1A):c.1940+5G>A	rs753866885	0.00003

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