ClinVar Miner

List of variants in gene GRIN2A reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_001134407.3(GRIN2A):c.1251C>A (p.Val417=) rs139329447
NM_001134407.3(GRIN2A):c.1251C>T (p.Val417=) rs139329447
NM_001134407.3(GRIN2A):c.1329-8C>T rs7193290
NM_001134407.3(GRIN2A):c.1329-9T>G rs541442732
NM_001134407.3(GRIN2A):c.1629C>T (p.Thr543=) rs758378272
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382
NM_001134407.3(GRIN2A):c.2250C>T (p.Ile750=) rs143779792
NM_001134407.3(GRIN2A):c.225C>T (p.Asn75=) rs527686036
NM_001134407.3(GRIN2A):c.2331G>A (p.Leu777=) rs118035164
NM_001134407.3(GRIN2A):c.2532G>A (p.Lys844=) rs754414929
NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=) rs569998469
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465
NM_001134407.3(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995
NM_001134407.3(GRIN2A):c.3622C>A (p.Arg1208=) rs78544202
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464
NM_001134407.3(GRIN2A):c.669C>T (p.His223=) rs138117658
NM_001134407.3(GRIN2A):c.900C>T (p.Thr300=) rs143669998
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448

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