List of variants in gene F2 reported as not provided for hematologic disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000506.5(F2):c.1726-59G>A	rs3136516	0.38221
NM_000506.5(F2):c.*97G>A	rs1799963	0.00979
NM_000506.5(F2):c.*96C>T	rs72550707	0.00093
NM_000506.5(F2):c.1621C>T (p.Arg541Trp)	rs886048338
NM_000506.5(F2):c.1787G>T (p.Arg596Leu)	rs387907201

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