List of variants in gene F5 reported as benign for Thrombophilia due to activated protein C resistance

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.5290A>G (p.Met1764Val)	rs6030	0.29437
NM_000130.4(F5):c.1601G>A (p.Arg534Gln)	rs6025	0.01762
NM_000130.5(F5):c.5245C>G (p.Leu1749Val)	rs6034	0.00144
NM_000130.5(F5):c.4589A>C (p.Glu1530Ala)	rs6007	0.00140
NM_000130.5(F5):c.5646G>A (p.Trp1882Ter)	rs1557908012

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