List of variants in gene F13B reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001994.3(F13B):c.456A>G (p.Thr152=)	rs5997	0.77286
NM_001994.3(F13B):c.344G>A (p.Arg115His)	rs6003	0.75658
NM_001994.3(F13B):c.1806T>C (p.Asn602=)	rs5998	0.42860
NM_001994.3(F13B):c.*143G>A	rs698859	0.31980

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