List of variants in gene F5 reported as uncertain significance for habitual spontaneous abortion

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.5265A>G (p.Ile1755Met)	rs41272455	0.00113
NM_000130.5(F5):c.4309A>T (p.Thr1437Ser)	rs115148599	0.00026
NM_000130.5(F5):c.4796+3T>C

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