List of variants in gene MTMR2 reported as likely benign for not provided

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_016156.6(MTMR2):c.186+5591A>G	rs61903339	0.01687
NM_016156.6(MTMR2):c.654+77C>T	rs143256055	0.01541
NM_016156.6(MTMR2):c.469-147C>T	rs139704398	0.01525
NM_016156.6(MTMR2):c.1480-220G>A	rs117909641	0.01522
NM_016156.6(MTMR2):c.*85A>C	rs578159	0.01009
NM_016156.6(MTMR2):c.358-60G>C	rs116463605	0.00970
NM_016156.6(MTMR2):c.994-21A>G	rs199703270	0.00779
NM_016156.6(MTMR2):c.805-137T>C	rs146008052	0.00730
NM_016156.6(MTMR2):c.262+198del	rs59229676	0.00717
NM_016156.6(MTMR2):c.*163G>A	rs114078363	0.00643
NM_016156.6(MTMR2):c.1386+151dup	rs111800867	0.00396
NM_016156.6(MTMR2):c.130G>A (p.Val44Ile)	rs146004831	0.00293
NM_016156.6(MTMR2):c.1488C>T (p.Thr496=)	rs112327353	0.00216
NM_016156.6(MTMR2):c.187-59G>C	rs182991283	0.00177
NM_016156.6(MTMR2):c.1855T>C (p.Ser619Pro)	rs116750638	0.00169
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.1862G>A (p.Arg621Gln)	rs371925152	0.00002
NM_016156.6(MTMR2):c.1218A>C (p.Val406=)	rs2135426567
NM_016156.6(MTMR2):c.1398T>C (p.His466=)	rs1590974679
NM_016156.6(MTMR2):c.1480-4_1480-3insA	rs752523757
NM_016156.6(MTMR2):c.184_186del (p.Arg62del)	rs141498429
NM_016156.6(MTMR2):c.186+5624TTTTA[5]
NM_016156.6(MTMR2):c.186+733del	rs34689209
NM_016156.6(MTMR2):c.1929A>G (p.Val643=)	rs779529851
NM_016156.6(MTMR2):c.357+10A>G	rs1590997402
NM_016156.6(MTMR2):c.804+301T>G	rs138909020
NM_016156.6(MTMR2):c.805-140dup	rs373012424

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