List of variants in gene F2 reported as likely benign for Thrombophilia due to thrombin defect

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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_000506.5(F2):c.494C>T (p.Thr165Met)	rs5896	0.13207
NM_000506.5(F2):c.1233G>A (p.Pro411=)	rs5898	0.06671
NM_000506.5(F2):c.480C>T (p.Pro160=)	rs3136452	0.04324
NM_000506.5(F2):c.79+7G>A	rs3136431	0.02419
NM_000506.5(F2):c.423-7G>C	rs2070852

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