List of variants reported as benign for Intellectual disability, autosomal dominant 13

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.13080T>C (p.Thr4360=)	rs13749	0.29638
NM_001376.5(DYNC1H1):c.13372+9G>A	rs1004903	0.29092
NM_001376.5(DYNC1H1):c.4396-25A>G	rs2251644	0.20858
NM_001376.5(DYNC1H1):c.8344-30G>A	rs2180510	0.20528
NM_001376.5(DYNC1H1):c.1462-41G>A	rs2983422	0.19200
NM_001376.5(DYNC1H1):c.624G>A (p.Pro208=)	rs3818188	0.17021
NM_001376.5(DYNC1H1):c.3333+23A>G	rs4900529	0.15653
NM_001376.5(DYNC1H1):c.3600A>G (p.Gln1200=)	rs12893215	0.15549
NM_001376.5(DYNC1H1):c.8928A>G (p.Leu2976=)	rs8010870	0.14754
NM_001376.5(DYNC1H1):c.962-15dup	rs3830914

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