List of variants in gene DYNC1H1 reported as likely pathogenic for Inborn genetic diseases

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10051A>T (p.Ile3351Phe)	rs1567018763
NM_001376.5(DYNC1H1):c.11083C>T (p.Arg3695Trp)	rs2503843400
NM_001376.5(DYNC1H1):c.4366G>A (p.Glu1456Lys)	rs2503730449
NM_001376.5(DYNC1H1):c.5645C>A (p.Thr1882Asn)	rs2503742080
NM_001376.5(DYNC1H1):c.5885G>A (p.Arg1962His)	rs1057518287
NM_001376.5(DYNC1H1):c.6268C>T (p.Leu2090Phe)	rs2503751910
NM_001376.5(DYNC1H1):c.6989G>A (p.Gly2330Glu)	rs1555410010

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