List of variants in gene MTMR2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_016156.6(MTMR2):c.1634A>G (p.Asn545Ser)	rs558018	0.01295
NM_016156.6(MTMR2):c.*1684A>C	rs79576160	0.00401
NM_016156.6(MTMR2):c.570+11T>C	rs182582445	0.00390
NM_016156.6(MTMR2):c.*837G>A	rs532069328	0.00323
NM_016156.6(MTMR2):c.*2187A>G	rs141738388	0.00241
NM_016156.6(MTMR2):c.1488C>T (p.Thr496=)	rs112327353	0.00216
NM_016156.6(MTMR2):c.1805C>G (p.Ala602Gly)	rs76784113	0.00069
NM_016156.6(MTMR2):c.*1089C>G	rs147982779	0.00031
NM_016156.6(MTMR2):c.1862G>A (p.Arg621Gln)	rs371925152	0.00002
NM_016156.6(MTMR2):c.240A>C (p.Pro80=)	rs201920176	0.00001

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