List of variants in gene TCOF1 reported as benign by Genetics Laboratories, Oxford Radcliffe Hospitals NHS Trust

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_001371623.1(TCOF1):c.1083+39G>A	rs56113366	0.05067
NM_001371623.1(TCOF1):c.305-52A>G	rs41287124	0.01012
NM_001371623.1(TCOF1):c.1278+60G>C	rs143713714	0.00827
NM_001371623.1(TCOF1):c.2859+3303G>A	rs112447402	0.00742
NM_001371623.1(TCOF1):c.4443+108C>A	rs111365835	0.00548

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