List of variants in gene MCFD2 reported as likely benign for coagulation protein disease

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_139279.6(MCFD2):c.*2761T>C	rs193204253	0.01332
NM_139279.6(MCFD2):c.*1407C>T	rs138459734	0.00806
NM_139279.6(MCFD2):c.310-11G>C	rs144139062	0.00567
NM_139279.6(MCFD2):c.*569G>A	rs149363149	0.00473
NM_139279.6(MCFD2):c.*354C>T	rs191255002	0.00396
NM_139279.6(MCFD2):c.*557G>A	rs185756640	0.00078

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