List of variants in gene F11 reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.595+11A>G	rs534170853	0.00001
NM_000128.4(F11):c.1207G>T (p.Val403Leu)	rs281875266
NM_000128.4(F11):c.26A>G (p.His9Arg)	rs774676239

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