List of variants in gene MYT1L reported as likely pathogenic by Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001303052.2(MYT1L):c.1975C>T (p.Arg659Ter)	rs745333246
NM_001303052.2(MYT1L):c.3076C>A (p.Arg1026Ser)	rs1558710588
NM_001303052.2(MYT1L):c.535C>T (p.Arg179Ter)	rs1558414255

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