List of variants in gene F11 reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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_000128.4(F11):c.1858G>C (p.Glu620Gln)	rs148054334	0.00010
NM_000128.4(F11):c.783G>C (p.Glu261Asp)	rs201079681	0.00007
NM_000128.4(F11):c.802C>T (p.Arg268Cys)	rs763496524	0.00005
NM_000128.4(F11):c.599G>A (p.Cys200Tyr)	rs757817254	0.00001
NM_000128.4(F11):c.1288G>T (p.Ala430Ser)	rs753909969

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