Variants in gene FBXL4 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001278716.2(FBXL4):c.1232G>A (p.Cys411Tyr)	rs773850151	0.00014
NM_001278716.2(FBXL4):c.616C>T (p.Arg206Ter)	rs964532159	0.00006
NM_001278716.2(FBXL4):c.64C>T (p.Arg22Ter)	rs200440128	0.00005
NM_001278716.2(FBXL4):c.1288C>T (p.Arg430Ter)	rs758395213	0.00003
NM_001278716.2(FBXL4):c.1444C>T (p.Arg482Trp)	rs398123061	0.00003
NM_001278716.2(FBXL4):c.1790A>C (p.Gln597Pro)	rs201989042	0.00001
NM_001278716.2(FBXL4):c.292C>T (p.Arg98Ter)	rs1554222130	0.00001
NM_001278716.2(FBXL4):c.419T>C (p.Val140Ala)	rs1057519447	0.00001
NM_001278716.2(FBXL4):c.1067del (p.Gly356fs)	rs1554219474
NM_001278716.2(FBXL4):c.1694A>G (p.Asp565Gly)	rs398123062
NM_001278716.2(FBXL4):c.1698A>G (p.Ile566Met)	rs1554215959
NM_001278716.2(FBXL4):c.1703G>C (p.Gly568Ala)	rs398123060
NM_001278716.2(FBXL4):c.219T>A (p.Tyr73Ter)	rs747536886
NM_001278716.2(FBXL4):c.486T>A (p.Tyr162Ter)	rs1562245046

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