List of variants in gene MMAA reported as likely benign for Methylmalonic acidemia

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_172250.3(MMAA):c.*4119del	rs200143270	0.01489
NM_172250.3(MMAA):c.630A>G (p.Pro210=)	rs374347679	0.00017
NM_172250.3(MMAA):c.*1952dup	rs150630369
NM_172250.3(MMAA):c.2622_2625del	rs60186480
NM_172250.3(MMAA):c.*3274del	rs33978754

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