List of variants in gene MTMR2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_016156.6(MTMR2):c.279T>C (p.Tyr93=)	rs372937811	0.00009
NM_016156.6(MTMR2):c.298G>A (p.Ala100Thr)	rs370701984	0.00008
NM_016156.6(MTMR2):c.1218A>C (p.Val406=)	rs2135426567
NM_016156.6(MTMR2):c.186+5624TTTTA[5]

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