List of variants in gene GRIN2A reported as uncertain significance 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: 20

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser)	rs77029288	0.00068
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly)	rs145063086	0.00067
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=)	rs372083517	0.00022
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg)	rs183029507	0.00007
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile)	rs367543124	0.00006
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=)	rs113847665	0.00004
NM_001134407.3(GRIN2A):c.883G>A (p.Gly295Ser)	rs568484876	0.00004
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp)	rs75761674	0.00003
NM_001134407.3(GRIN2A):c.2543G>A (p.Cys848Tyr)	rs779911797	0.00002
NM_001134407.3(GRIN2A):c.3037C>T (p.Leu1013=)	rs775262289	0.00002
NM_001134407.3(GRIN2A):c.171C>T (p.Pro57=)	rs781693549	0.00001
NM_001134407.3(GRIN2A):c.3619T>C (p.Tyr1207His)	rs587780355	0.00001
NM_001134407.3(GRIN2A):c.495T>C (p.Tyr165=)	rs569491666	0.00001
NM_001134407.3(GRIN2A):c.1329-7dup	rs1455515948
NM_001134407.3(GRIN2A):c.1374G>A (p.Gly458=)	rs368221866
NM_001134407.3(GRIN2A):c.3064C>A (p.Arg1022Ser)	rs560057284
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr)	rs375160358
NM_001134407.3(GRIN2A):c.3785C>T (p.Thr1262Ile)	rs587780351
NM_001134407.3(GRIN2A):c.4081C>G (p.His1361Asp)	rs797045606
NM_001134407.3(GRIN2A):c.415G>T (p.Asp139Tyr)	rs1555455852

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