List of variants in gene LMOD3 reported as benign by Invitae

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_198271.5(LMOD3):c.642G>A (p.Ser214=)	rs9815992	0.04475
NM_198271.5(LMOD3):c.1270T>C (p.Leu424=)	rs72924884	0.03865
NM_198271.5(LMOD3):c.759T>C (p.Pro253=)	rs115972674	0.02947
NM_198271.5(LMOD3):c.878G>A (p.Gly293Asp)	rs111797345	0.01530
NM_198271.5(LMOD3):c.1226A>G (p.Gln409Arg)	rs116257053	0.01432
NM_198271.5(LMOD3):c.1679C>T (p.Ala560Val)	rs17005363	0.01345
NM_198271.5(LMOD3):c.1655C>A (p.Pro552His)	rs145387235	0.01335
NM_198271.5(LMOD3):c.1144C>T (p.Pro382Ser)	rs74350755	0.00814
NM_198271.5(LMOD3):c.1313A>T (p.Lys438Met)	rs6810145	0.00516
NM_198271.5(LMOD3):c.1493G>A (p.Arg498Gln)	rs116440123	0.00513
NM_198271.5(LMOD3):c.1257G>C (p.Met419Ile)	rs75713718	0.00383
NM_198271.5(LMOD3):c.837G>A (p.Lys279=)	rs185967498	0.00138
NM_198271.5(LMOD3):c.1657-14T>C	rs200984574	0.00137
NM_198271.5(LMOD3):c.1617A>G (p.Leu539=)	rs374084990	0.00003
NM_198271.5(LMOD3):c.426A>C (p.Glu142Asp)	rs111848977
NM_198271.5(LMOD3):c.426A>G (p.Glu142=)	rs111848977

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