Variants in gene TPM1 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001018005.2(TPM1):c.389T>C (p.Ile130Thr)	rs727503517
NM_001018005.2(TPM1):c.602C>T (p.Thr201Met)	rs730881141
NM_001018005.2(TPM1):c.725C>T (p.Ala242Val)	rs397516387

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