ClinVar Miner

List of variants in gene GRIN2B reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_000834.4(GRIN2B):c.*1074C>T rs201335778
NM_000834.4(GRIN2B):c.*219C>T rs80081965
NM_000834.4(GRIN2B):c.*409T>G rs890
NM_000834.4(GRIN2B):c.*567A>C rs1805503
NM_000834.4(GRIN2B):c.*988A>G rs1805477
NM_000834.4(GRIN2B):c.-15G>A rs12818068
NM_000834.4(GRIN2B):c.1126-12A>G rs76777620
NM_000834.4(GRIN2B):c.15G>A (p.Ala5=) rs34315573
NM_000834.4(GRIN2B):c.1665C>T (p.Ser555=) rs1805482
NM_000834.4(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.4(GRIN2B):c.2514C>T (p.Cys838=) rs3026160
NM_000834.4(GRIN2B):c.2664C>T (p.Thr888=) rs1806201
NM_000834.4(GRIN2B):c.2691C>T (p.Asn897=) rs35125534
NM_000834.4(GRIN2B):c.3534C>T (p.His1178=) rs1806191
NM_000834.4(GRIN2B):c.366C>G (p.Pro122=) rs7301328
NM_000834.4(GRIN2B):c.4197T>C (p.His1399=) rs1805247
NM_000834.4(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246
NM_000834.4(GRIN2B):c.504C>A (p.Ile168=) rs36031537
NM_000834.4(GRIN2B):c.870C>T (p.Pro290=) rs1124894

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