List of variants in gene GRIN2B reported by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000834.5(GRIN2B):c.366C>G (p.Pro122=)	rs7301328	0.41972
NM_000834.5(GRIN2B):c.3534C>T (p.His1178=)	rs1806191	0.39095
NM_000834.5(GRIN2B):c.1665C>T (p.Ser555=)	rs1805482	0.26553
NM_000834.5(GRIN2B):c.2664C>T (p.Thr888=)	rs1806201	0.23527
NM_000834.5(GRIN2B):c.3498C>T (p.Ser1166=)	rs45600931	0.00538
NM_000834.5(GRIN2B):c.228C>T (p.Thr76=)	rs77299791	0.00070
NM_000834.5(GRIN2B):c.1851C>T (p.Ser617=)	rs147373250	0.00045
NM_000834.5(GRIN2B):c.2481G>A (p.Ala827=)	rs189384622	0.00015
NM_000834.5(GRIN2B):c.2172G>T (p.Gly724=)	rs200813905
NM_000834.5(GRIN2B):c.2252T>C (p.Ile751Thr)	rs876661055
NM_000834.5(GRIN2B):c.2459G>C (p.Gly820Ala)	rs797044849

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