List of variants in gene MTMR2 reported as pathogenic by OMIM

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_016156.6(MTMR2):c.1276C>T (p.Gln426Ter)	rs121434402	0.00001
NM_016156.6(MTMR2):c.1444C>T (p.Gln482Ter)	rs121434404
NM_016156.6(MTMR2):c.1593+1G>A	rs1590970875
NM_016156.6(MTMR2):c.1736_1745delinsCC (p.Tyr579fs)	rs1863269109
NM_016156.6(MTMR2):c.826G>T (p.Glu276Ter)	rs121434403

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