List of variants in gene TPM3 reported as benign for Congenital myopathy 4B, autosomal recessive

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_152263.4(TPM3):c.776-49T>C	rs4845364	0.62914
NM_152263.4(TPM3):c.*2409G>C	rs142369480	0.01324
NM_152263.4(TPM3):c.*1791G>A	rs114799756	0.01140
NM_152263.4(TPM3):c.*2069C>T	rs140536164	0.00588
NM_152263.4(TPM3):c.*1291A>G	rs375670563	0.00094

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