List of variants in gene F7 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.142C>T (p.Pro48Ser)	rs373376565	0.00050
NM_019616.4(F7):c.364+14T>G
NM_019616.4(F7):c.605G>A (p.Cys202Tyr)

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