List of variants in gene GBE1 reported as benign 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000158.4(GBE1):c.1000A>G (p.Ile334Val)	rs2172397	0.97909
NM_000158.4(GBE1):c.568A>G (p.Arg190Gly)	rs2229519	0.29724
NM_000158.4(GBE1):c.143+10G>T	rs9820490	0.12510
NM_000158.4(GBE1):c.579G>A (p.Lys193=)	rs17019144	0.09257
NM_000158.4(GBE1):c.342C>T (p.Tyr114=)	rs13320194	0.08854
NM_000158.4(GBE1):c.1519A>G (p.Thr507Ala)	rs2228389	0.06703
NM_000158.4(GBE1):c.1716C>T (p.Asp572=)	rs2229520	0.01610
NM_000158.4(GBE1):c.176T>C (p.Ile59Thr)	rs28763904	0.00604
NM_000158.4(GBE1):c.118C>A (p.Pro40Thr)	rs35196441	0.00569
NM_000158.4(GBE1):c.2017G>A (p.Ala673Thr)	rs193074572	0.00529
NM_000158.4(GBE1):c.839G>A (p.Gly280Asp)	rs28763902	0.00388

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