List of variants in gene MTM1 reported as 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000252.3(MTM1):c.1054-201A>T	rs222408	0.29752
NM_000252.3(MTM1):c.1054-193A>G	rs222409	0.27851
NM_000252.3(MTM1):c.-10-328A>G	rs2138413	0.26655
NM_000252.3(MTM1):c.867+180A>C	rs222368	0.15351
NM_000252.3(MTM1):c.528+70G>A	rs16995740	0.12756
NM_000252.3(MTM1):c.232-147G>C	rs10521888	0.12583
NM_000252.3(MTM1):c.342+106C>G	rs222394	0.03885
NM_000252.3(MTM1):c.232-28C>T	rs73620649	0.03576
NM_000252.3(MTM1):c.1260+240A>G	rs147799230	0.01980
NM_000252.3(MTM1):c.64-50A>T	rs201279564	0.00136
NM_000252.3(MTM1):c.339T>C (p.Cys113=)	rs147644722	0.00111
NM_000252.3(MTM1):c.1053+23T>C	rs180775341	0.00057
NM_000252.3(MTM1):c.1052A>G (p.Lys351Arg)	rs150430628	0.00022
NM_000252.3(MTM1):c.-10-152=	rs182630
NM_000252.3(MTM1):c.529-257C>G	rs55824675

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