List of variants in gene FBXL4 reported as uncertain significance for not specified

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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_001278716.2(FBXL4):c.1622C>T (p.Thr541Ile)	rs1391578014	0.00006
NM_001278716.2(FBXL4):c.1135C>T (p.Arg379Cys)	rs778692687	0.00005
NM_001278716.2(FBXL4):c.1025C>G (p.Ser342Cys)	rs780707718	0.00001
GRCh37/hg19 6q16.1(chr6:99331183-99393661)
NM_001278716.2(FBXL4):c.1252G>C (p.Ala418Pro)	rs542852839

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