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: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=)	rs9806806	0.33435
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=)	rs2229193	0.27838
NM_001134407.3(GRIN2A):c.1329-8C>T	rs7193290	0.01855
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=)	rs77705198	0.00059
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala)	rs138809301	0.00055
NM_001134407.3(GRIN2A):c.2277C>T (p.Thr759=)	rs148846694	0.00024
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn)	rs540445580	0.00006
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile)	rs587780353	0.00004
NM_001134407.3(GRIN2A):c.3624G>A (p.Arg1208=)	rs587780350	0.00003
NM_001134407.3(GRIN2A):c.2247C>T (p.Thr749=)	rs202026070	0.00001
NM_001134407.3(GRIN2A):c.3636G>A (p.Thr1212=)	rs765614514	0.00001
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=)	rs587780352	0.00001
NM_001134407.3(GRIN2A):c.1667C>T (p.Ser556Phe)	rs587780349
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.420G>A (p.Pro140=)	rs367543126
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met)	rs78631453

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