List of variants in gene F13A1 reported as likely benign for factor XIII deficiency

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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_000129.4(F13A1):c.1704A>G (p.Glu568=)	rs5986	0.07753
NM_000129.4(F13A1):c.*443G>A	rs3024486	0.04832
NM_000129.4(F13A1):c.*112G>T	rs3024463	0.04625
NM_000129.4(F13A1):c.614A>T (p.Tyr205Phe)	rs3024477	0.01940
NM_000129.4(F13A1):c.1689G>A (p.Gly563=)	rs58315745	0.00958
NM_000129.4(F13A1):c.1184C>T (p.Ala395Val)	rs76451285	0.00008
NM_000129.4(F13A1):c.-18-5dup	rs750373197

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