List of variants in gene MYOM1 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_003803.4(MYOM1):c.1643+156T>C	rs34628686	0.02228
NM_003803.4(MYOM1):c.1023-32C>T	rs78567624	0.01896
NM_003803.4(MYOM1):c.1174+124T>C	rs11873066	0.01760
NM_003803.4(MYOM1):c.1502-113G>A	rs74884432	0.01667
NM_003803.4(MYOM1):c.3419-263C>G	rs117267880	0.01286
NM_003803.4(MYOM1):c.91C>A (p.Arg31=)	rs76382984	0.01227
NM_003803.4(MYOM1):c.739G>A (p.Glu247Lys)	rs139422575	0.00435
NM_003803.4(MYOM1):c.772-225_772-224insG	rs1370710912	0.00340
NM_003803.4(MYOM1):c.1978C>G (p.Pro660Ala)	rs201104206	0.00100
NM_003803.4(MYOM1):c.-28-11T>C	rs78603353	0.00068
NM_003803.4(MYOM1):c.1023-280_1023-279dup	rs34464336
NM_003803.4(MYOM1):c.120C>A (p.Thr40=)	rs876657535
NM_003803.4(MYOM1):c.2992-45del
NM_003803.4(MYOM1):c.3441T>C (p.Asn1147=)	rs1598671900
NM_003803.4(MYOM1):c.3636A>T (p.Val1212=)	rs760952047
NM_003803.4(MYOM1):c.4138-7C>G	rs772811909
NM_003803.4(MYOM1):c.4251+240A>G
NM_003803.4(MYOM1):c.432-275del	rs35154072
NM_003803.4(MYOM1):c.432-276_432-275dup	rs35154072
NM_003803.4(MYOM1):c.772-221del	rs763218658
NM_003803.4(MYOM1):c.772-221dup	rs763218658
NM_003803.4(MYOM1):c.930-68GT[6]	rs202240743

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