List of variants in gene combination GLE1, LOC101929270 reported as uncertain significance for not provided

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001003722.2(GLE1):c.1393T>A (p.Ser465Thr)	rs141709685	0.00155
NM_001003722.2(GLE1):c.1641T>C (p.Tyr547=)	rs77053118	0.00031
NM_001003722.2(GLE1):c.*540G>A	rs886063492	0.00008
NM_001003722.2(GLE1):c.1724G>A (p.Arg575His)	rs190673897	0.00003
NM_001003722.2(GLE1):c.1808G>T (p.Arg603Leu)	rs376686581	0.00001
NM_001003722.2(GLE1):c.1894G>A (p.Ala632Thr)	rs1392638751	0.00001
NM_001003722.2(GLE1):c.1997G>T (p.Gly666Val)	rs1064793630	0.00001
NM_001003722.2(GLE1):c.1396G>A (p.Val466Ile)	rs72756895
NM_001003722.2(GLE1):c.1422C>A (p.Asp474Glu)
NM_001003722.2(GLE1):c.2093C>T (p.Ser698Phe)

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