Variants in gene MYOM1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_003803.4(MYOM1):c.91C>A (p.Arg31=)	rs76382984	0.01227
NM_003803.4(MYOM1):c.2384+4A>T	rs73373171	0.00286
NM_003803.4(MYOM1):c.2062A>T (p.Thr688Ser)	rs188677538	0.00276
NM_003803.4(MYOM1):c.2727G>A (p.Pro909=)	rs72860212	0.00188
NM_003803.4(MYOM1):c.1803C>T (p.Pro601=)	rs371861150	0.00153
NM_003803.4(MYOM1):c.1978C>G (p.Pro660Ala)	rs201104206	0.00100
NM_003803.4(MYOM1):c.924C>A (p.Val308=)	rs536739408

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