List of variants in gene F5 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.4923C>T (p.Leu1641=)	rs116809837	0.00272
NM_000130.5(F5):c.6554A>G (p.Lys2185Arg)	rs6679078	0.00271
NM_000130.5(F5):c.5431A>T (p.Met1811Leu)	rs138877178	0.00074
NM_000130.5(F5):c.885C>T (p.Thr295=)	rs148752831	0.00048
NM_000130.5(F5):c.5490G>A (p.Leu1830=)	rs149092241	0.00029
NM_000130.5(F5):c.5177G>A (p.Arg1726Gln)	rs369516642	0.00009
NM_000130.5(F5):c.6606T>A (p.Arg2202=)	rs368496361	0.00001
NM_000130.5(F5):c.510C>T (p.His170=)
NM_000130.5(F5):c.5598T>C (p.Pro1866=)
NM_000130.5(F5):c.5694G>A (p.Thr1898=)
NM_000130.5(F5):c.5949C>T (p.His1983=)
NM_000130.5(F5):c.6246C>T (p.Ile2082=)
NM_000130.5(F5):c.6489A>G (p.Glu2163=)

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