List of variants in gene GRIN2A reported as likely pathogenic by Invitae

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.1008-2A>G	rs2043686667
NM_001134407.3(GRIN2A):c.1328+2T>C	rs2042847630
NM_001134407.3(GRIN2A):c.1329-1G>C
NM_001134407.3(GRIN2A):c.1329-2A>C	rs2141346217
NM_001134407.3(GRIN2A):c.1382T>A (p.Ile461Asn)	rs1567337914
NM_001134407.3(GRIN2A):c.1630G>A (p.Val544Ile)	rs2141342055
NM_001134407.3(GRIN2A):c.1652-2A>G	rs2141325752
NM_001134407.3(GRIN2A):c.1777+1G>C	rs2141325180
NM_001134407.3(GRIN2A):c.1777+2T>C	rs2141325169
NM_001134407.3(GRIN2A):c.1904C>A (p.Ala635Asp)	rs2042448930
NM_001134407.3(GRIN2A):c.2007+1G>T
NM_001134407.3(GRIN2A):c.2075_2116dup (p.Arg692_Met705dup)	rs2141294782
NM_001134407.3(GRIN2A):c.2147C>T (p.Ala716Val)
NM_001134407.3(GRIN2A):c.2168+1G>C	rs2141294532
NM_001134407.3(GRIN2A):c.2314A>G (p.Lys772Glu)	rs1555488094
NM_001134407.3(GRIN2A):c.2326G>A (p.Asp776Asn)
NM_001134407.3(GRIN2A):c.2356+1G>T	rs2141230207
NM_001134407.3(GRIN2A):c.2357-2A>T
NM_001134407.3(GRIN2A):c.2365GAG[1] (p.Glu790del)
NM_001134407.3(GRIN2A):c.236C>G (p.Pro79Arg)	rs1250662891
NM_001134407.3(GRIN2A):c.255_256insCTCATGTCCGGG (p.His85_Val86insLeuMetSerGly)	rs2142389389
NM_001134407.3(GRIN2A):c.2658T>A (p.Asn886Lys)	rs1321794341
NM_001134407.3(GRIN2A):c.292C>T (p.Leu98Phe)	rs1596586969
NM_001134407.3(GRIN2A):c.4067C>G (p.Ser1356Cys)
NM_001134407.3(GRIN2A):c.415-2A>G	rs2141633312

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