List of variants in gene DYNC1H1 reported as not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.5971G>A (p.Asp1991Asn)	rs151001016	0.00027
NM_001376.5(DYNC1H1):c.2869-3C>T	rs750614475	0.00004
NM_001376.5(DYNC1H1):c.11503A>G (p.Ile3835Val)	rs148513391	0.00003
NM_001376.5(DYNC1H1):c.13414G>A (p.Gly4472Ser)	rs199692678	0.00002
NM_001376.5(DYNC1H1):c.13777G>A (p.Val4593Ile)	rs750566844	0.00001
NM_001376.5(DYNC1H1):c.11989C>T (p.Arg3997Trp)	rs1399236395
NM_001376.5(DYNC1H1):c.1859A>G (p.His620Arg)	rs2503694662
NM_001376.5(DYNC1H1):c.3278T>C (p.Phe1093Ser)	rs1555408829
NM_001376.5(DYNC1H1):c.3504del (p.Phe1169fs)	rs2141281091
NM_001376.5(DYNC1H1):c.4376T>C (p.Leu1459Ser)	rs2503730471
NM_001376.5(DYNC1H1):c.5114T>C (p.Val1705Ala)	rs2048178354
NM_001376.5(DYNC1H1):c.5884C>T (p.Arg1962Cys)	rs879253881
NM_001376.5(DYNC1H1):c.917A>G (p.His306Arg)	rs387906738
NM_001376.5(DYNC1H1):c.9959C>T (p.Ala3320Val)	rs1555411305

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