List of variants in gene GLE1 reported as benign for multiple congenital anomalies/dysmorphic syndrome

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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_001003722.2(GLE1):c.727A>G (p.Ile243Val)	rs2275260	0.26894
NM_001003722.2(GLE1):c.99+29C>G	rs56164320	0.04523
NM_001003722.2(GLE1):c.1000G>A (p.Glu334Lys)	rs138310419	0.01201
NM_001003722.2(GLE1):c.433-15A>C	rs752897261	0.00213
NM_001003722.2(GLE1):c.1242+30G>T	rs869455

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