List of variants in gene DNM1 reported as likely pathogenic for 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004408.4(DNM1):c.1037G>A (p.Gly346Asp)
NM_004408.4(DNM1):c.1067T>G (p.Leu356Arg)	rs1835085404
NM_004408.4(DNM1):c.1072G>T (p.Gly358Trp)	rs1064794828
NM_004408.4(DNM1):c.1169A>C (p.Tyr390Ser)	rs1064795538
NM_004408.4(DNM1):c.1180A>G (p.Asn394Asp)	rs1835103161
NM_004408.4(DNM1):c.1603A>G (p.Lys535Glu)	rs1554781545
NM_004408.4(DNM1):c.1607G>A (p.Gly536Glu)	rs754404446
NM_004408.4(DNM1):c.854T>A (p.Leu285Gln)	rs1131691877

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