ClinVar Miner

List of variants in gene MTMR2 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_016156.6(MTMR2):c.186+575A>G rs570127 0.97023
NM_016156.6(MTMR2):c.263-164A>G rs552334 0.63673
NM_016156.6(MTMR2):c.262+136T>C rs687559 0.60988
NM_016156.6(MTMR2):c.1770+129C>T rs499637 0.60639
NM_016156.6(MTMR2):c.468+325T>C rs523049 0.59952
NM_016156.6(MTMR2):c.1593+297C>T rs523153 0.35427
NM_016156.6(MTMR2):c.81-298G>A rs483176 0.29294
NM_016156.6(MTMR2):c.1131C>T (p.Thr377=) rs566204 0.28363
NM_016156.6(MTMR2):c.1770+59T>G rs627568 0.28209
NM_016156.6(MTMR2):c.1386+188A>G rs580255 0.28136
NM_016156.6(MTMR2):c.655-82T>C rs474442 0.27768
NM_016156.6(MTMR2):c.8A>C (p.Lys3Thr) rs3824874 0.27654
NM_016156.6(MTMR2):c.469-76T>C rs11021336 0.14609
NM_016156.6(MTMR2):c.570+344G>A rs7107251 0.14377
NM_016156.6(MTMR2):c.1386+192G>C rs12274927 0.13955
NM_016156.6(MTMR2):c.1594-42C>T rs9919542 0.12925
NM_016156.6(MTMR2):c.1180-271T>A rs3789963 0.07662
NM_016156.6(MTMR2):c.186+155A>G rs518550 0.06113
NM_016156.6(MTMR2):c.1756C>A (p.Arg586=) rs61735577 0.04066
NM_016156.6(MTMR2):c.1504G>C (p.Glu502Gln) rs61735578 0.03636
NM_016156.6(MTMR2):c.654+230C>T rs113524244 0.03506
NM_016156.6(MTMR2):c.80+165G>A rs112880403 0.02981
NM_016156.6(MTMR2):c.357+45_357+48del rs371629162 0.02888
NM_016156.6(MTMR2):c.80+13C>T rs139510268 0.01848
NM_016156.6(MTMR2):c.1233G>A (p.Thr411=) rs113897932 0.01619
NM_016156.6(MTMR2):c.1634A>G (p.Asn545Ser) rs558018 0.01295
NM_016156.6(MTMR2):c.570+11T>C rs182582445 0.00390
NM_016156.6(MTMR2):c.1855T>C (p.Ser619Pro) rs116750638 0.00169
NM_016156.6(MTMR2):c.1805C>G (p.Ala602Gly) rs76784113 0.00069
NM_016156.6(MTMR2):c.1387-150C>G rs113173012
NM_016156.6(MTMR2):c.1771-142G>T rs473852
NM_016156.6(MTMR2):c.186+19A>T rs12385798
NM_016156.6(MTMR2):c.186+5624TTTTA[6] rs112378876
NM_016156.6(MTMR2):c.186+724dup rs34689209
NM_016156.6(MTMR2):c.187-235dup rs61523739
NM_016156.6(MTMR2):c.263-59G>T rs551367
NM_016156.6(MTMR2):c.655-285dup rs36142511

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