List of variants in gene GRIN2B reported as not provided 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000834.5(GRIN2B):c.2664C>T (p.Thr888=)	rs1806201	0.23527
NM_000834.5(GRIN2B):c.4197T>C (p.His1399=)	rs1805247	0.16667
NM_000834.5(GRIN2B):c.15G>A (p.Ala5=)	rs34315573	0.03193
NM_000834.5(GRIN2B):c.4218C>T (p.Phe1406=)	rs1805246	0.02603
NM_000834.5(GRIN2B):c.2691C>T (p.Asn897=)	rs35125534	0.01112
NM_000834.5(GRIN2B):c.1341C>T (p.Asp447=)	rs35025065	0.00902
NM_000834.5(GRIN2B):c.4240G>T (p.Ala1414Ser)	rs140744818	0.00085
NM_000834.5(GRIN2B):c.3648C>T (p.Arg1216=)	rs201405157	0.00016
NM_000834.5(GRIN2B):c.2712G>A (p.Thr904=)	rs199843136	0.00014
NM_000834.5(GRIN2B):c.2313G>A (p.Gly771=)	rs150554184	0.00003
NM_000834.5(GRIN2B):c.1833T>C (p.Gly611=)	rs367543148	0.00002
NM_000834.5(GRIN2B):c.14C>T (p.Ala5Val)	rs367543147	0.00001
NM_000834.5(GRIN2B):c.3562G>A (p.Gly1188Ser)	rs367543149	0.00001
NM_000834.5(GRIN2B):c.465C>A (p.Ser155=)	rs115189840

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