List of variants in gene MTMR2 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
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.1106T>C (p.Ile369Thr)	rs200083635	0.00019
NM_016156.6(MTMR2):c.1741A>G (p.Ile581Val)	rs149476960	0.00010
NM_016156.6(MTMR2):c.894A>T (p.Glu298Asp)	rs200898934	0.00007
NM_016156.6(MTMR2):c.356G>A (p.Arg119Gln)	rs759086106	0.00002
NM_016156.6(MTMR2):c.146C>G (p.Ser49Cys)	rs1170327910	0.00001
NM_016156.6(MTMR2):c.1661C>T (p.Pro554Leu)	rs750110066	0.00001
NM_016156.6(MTMR2):c.213A>G (p.Ala71=)	rs1402885565	0.00001
NM_016156.6(MTMR2):c.184_186del (p.Arg62del)	rs141498429
NM_016156.6(MTMR2):c.94C>G (p.His32Asp)	rs1591025020

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