List of variants in gene F5 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.319G>C (p.Asp107His)	rs6019	0.14054
NM_000130.5(F5):c.1238T>C (p.Met413Thr)	rs6033	0.06350
NM_000130.5(F5):c.3438C>G (p.His1146Gln)	rs6005	0.02373
NM_000130.5(F5):c.2925C>T (p.Pro975=)	rs41272457	0.01542
NM_000130.5(F5):c.2743A>T (p.Thr915Ser)	rs9332695	0.01344
NM_000130.5(F5):c.*476C>T	rs72708017	0.01259
NM_000130.5(F5):c.816C>T (p.Asn272=)	rs9332578	0.01203
NM_000130.5(F5):c.5460G>A (p.Met1820Ile)	rs6026	0.00789
NM_000130.5(F5):c.*376A>T	rs76510731	0.00746
NM_000130.5(F5):c.158+13T>C	rs116416322	0.00733
NM_000130.5(F5):c.*1488T>C	rs75764442	0.00676
NM_000130.5(F5):c.*1290G>A	rs9332677	0.00480
NM_000130.5(F5):c.6309G>A (p.Leu2103=)	rs35369423	0.00361
NM_000130.5(F5):c.2906A>G (p.Asn969Ser)	rs9332604	0.00302
NM_000130.5(F5):c.*2037G>A	rs550454517	0.00246
NM_000130.5(F5):c.3776C>A (p.Ser1259Tyr)	rs150104888	0.00246
NM_000130.5(F5):c.*581C>A	rs180742904	0.00227
NM_000130.5(F5):c.6193+7T>A	rs185294741	0.00156
NM_000130.5(F5):c.5054C>G (p.Thr1685Ser)	rs6011	0.00144
NM_000130.5(F5):c.3851C>T (p.Thr1284Ile)	rs139573207	0.00142
NM_000130.5(F5):c.3504A>C (p.Thr1168=)	rs13306332	0.00077
NM_000130.5(F5):c.5558G>T (p.Gly1853Val)	rs182566496	0.00039
NM_000130.5(F5):c.*838T>C	rs376103455	0.00016
NM_000130.5(F5):c.524A>G (p.His175Arg)	rs201510575	0.00016
NM_000130.5(F5):c.3952C>A (p.Gln1318Lys)	rs538359973	0.00001

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