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:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP
NM_000833.5(GRIN2A):c.1667C>T (p.Ser556Phe)	rs587780349
NM_000833.5(GRIN2A):c.3246C>G (p.Thr1082=)	rs143039009
NM_000833.5(GRIN2A):c.3553A>G (p.Lys1185Glu)	rs587780354
NM_000833.5(GRIN2A):c.3624G>A (p.Arg1208=)	rs587780350
NM_000833.5(GRIN2A):c.420G>A (p.Pro140=)	rs367543126
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=)	rs2229193
NM_001134407.3(GRIN2A):c.1329-8C>T	rs7193290
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.402C>T (p.Ile134=)	rs587780352
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met)	rs78631453
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile)	rs587780353
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg)	rs61731464

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