List of variants in gene PCCB reported as benign for not specified

Minimum submission review status:		Collection method:
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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000532.5(PCCB):c.967-46A>G	rs9833162	0.36992
NM_000532.5(PCCB):c.654+20T>C	rs3821445	0.15527
NM_000532.5(PCCB):c.967-42G>C	rs77495412	0.00769
NM_000532.4(PCCB):c.-37C>T	rs145734157	0.00591
NM_000532.5(PCCB):c.372+31T>C	rs16843829	0.00526
NM_000532.5(PCCB):c.1499-48A>G	rs144001285	0.00234
NM_000532.5(PCCB):c.184-12G>T	rs181283691	0.00185
NM_000532.5(PCCB):c.49C>A (p.Leu17Met)	rs200185747	0.00172

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