List of variants in gene combination LOC130057222, TPM1 reported as likely benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001018005.2(TPM1):c.240+4118C>G	rs140483658	0.02617
NM_001018005.2(TPM1):c.240+4218C>T	rs62013182	0.01724
NM_001018005.2(TPM1):c.240+4332del	rs146654937	0.00988
NM_001018005.2(TPM1):c.240+4268A>C	rs554540382	0.00733
NM_001018005.2(TPM1):c.240+4092C>G	rs151274957	0.00107
NM_001018005.2(TPM1):c.240+4465C>G	rs730881129	0.00001
NM_001018005.2(TPM1):c.240+4638C>T	rs567601554

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