List of variants in gene MMADHC reported as not provided for hematologic disorder

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_015702.3(MMADHC):c.133dup (p.Ala45fs)	rs864309740
NM_015702.3(MMADHC):c.160C>T (p.Arg54Ter)	rs118204047
NM_015702.3(MMADHC):c.228dup (p.Asn77fs)	rs864309741
NM_015702.3(MMADHC):c.307_324dup (p.Leu103_Ser108dup)	rs397509362
NM_015702.3(MMADHC):c.455dup (p.Cys153fs)	rs864309743
NM_015702.3(MMADHC):c.57_64del (p.Cys19_Ser20insTer)	rs397509361
NM_015702.3(MMADHC):c.60_61insAT (p.Leu21fs)	rs864309742

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