Variants in gene F11 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_000128.4(F11):c.1717-48A>G	rs5966	0.06916
NM_000128.4(F11):c.-54G>A	rs4253814	0.01170
NM_000128.4(F11):c.1016G>T (p.Cys339Phe)	rs5967	0.00586
NM_000128.4(F11):c.731A>G (p.Gln244Arg)	rs5969	0.00564
NM_000128.4(F11):c.*1A>G	rs143899287	0.00378
NM_000128.4(F11):c.1304+12G>A	rs116667976	0.00295
NM_000128.4(F11):c.453C>T (p.Tyr151=)	rs34807019	0.00248
NM_000128.4(F11):c.1305-9G>T	rs4253426	0.00153
NM_000128.4(F11):c.663C>T (p.Pro221=)	rs142846329	0.00120
NM_000128.4(F11):c.1020C>T (p.Asn340=)	rs149052026	0.00100
NM_000128.4(F11):c.1481-34G>T	rs2289253
NM_000128.4(F11):c.1576+51C>A	rs2289254

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