ClinVar Miner

List of variants in gene GRIN2A reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=) rs2229193
NM_001134407.3(GRIN2A):c.1329-8C>T rs7193290
NM_001134407.3(GRIN2A):c.1667C>T (p.Ser556Phe) rs587780349
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=) rs9806806
NM_001134407.3(GRIN2A):c.2277C>T (p.Thr759=) rs148846694
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=) rs77705198
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn) rs540445580
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301
NM_001134407.3(GRIN2A):c.3246C>G (p.Thr1082=) rs143039009
NM_001134407.3(GRIN2A):c.3553A>G (p.Lys1185Glu) rs587780354
NM_001134407.3(GRIN2A):c.3624G>A (p.Arg1208=) rs587780350
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=) rs587780352
NM_001134407.3(GRIN2A):c.420G>A (p.Pro140=) rs367543126
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353

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