List of variants in gene DYNC1H1 reported as uncertain significance by Inherited Neuropathy Consortium

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

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.1012G>A (p.Asp338Asn)	rs1555408131
NM_001376.5(DYNC1H1):c.1195A>G (p.Arg399Gly)	rs1595599240
NM_001376.5(DYNC1H1):c.1741A>C (p.Met581Leu)	rs1566999047
NM_001376.5(DYNC1H1):c.1750A>C (p.Ile584Leu)	rs387906741
NM_001376.5(DYNC1H1):c.1793G>T (p.Arg598Leu)	rs879254085
NM_001376.5(DYNC1H1):c.1808A>T (p.Glu603Val)	rs1595600898
NM_001376.5(DYNC1H1):c.1834G>A (p.Val612Met)	rs1555408333
NM_001376.5(DYNC1H1):c.2019G>C (p.Trp673Cys)	rs1555408345
NM_001376.5(DYNC1H1):c.3179T>C (p.Leu1060Ser)	rs1555408819
NM_001376.5(DYNC1H1):c.4808G>C (p.Arg1603Thr)	rs1555409418
NM_001376.5(DYNC1H1):c.7846G>A (p.Glu2616Lys)	rs1555410285
NM_001376.5(DYNC1H1):c.791G>A (p.Arg264Gln)	rs713993043
NM_001376.5(DYNC1H1):c.917A>G (p.His306Arg)	rs387906738

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