List of variants in gene GRIN1 reported as benign for not provided

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.570+263G>C	rs9411312	0.95742
NM_007327.4(GRIN1):c.394-22G>A	rs10870196	0.95430
NM_007327.4(GRIN1):c.1467+8G>A	rs10747050	0.95319
NM_007327.4(GRIN1):c.1467+202T>C	rs10870200	0.67192
NM_007327.4(GRIN1):c.1467+160G>A	rs11146026	0.55385
NM_007327.4(GRIN1):c.1340-38G>A	rs41290007	0.25388
NM_007327.4(GRIN1):c.968+274A>G	rs73571550	0.23874
NM_007327.4(GRIN1):c.789A>G (p.Pro263=)	rs6293	0.23665
NM_007327.4(GRIN1):c.672-80A>G	rs28687864	0.23545
NM_007327.4(GRIN1):c.672-134A>G	rs28514863	0.23502
NM_007327.4(GRIN1):c.394-139C>A	rs11146023	0.18358
NM_007327.4(GRIN1):c.394-176_394-175insA	rs71387806	0.15770
NM_007327.4(GRIN1):c.258+235C>T	rs2301363	0.14810
NM_007327.4(GRIN1):c.969-177G>A	rs28408401	0.04166
NM_007327.4(GRIN1):c.1467+182C>T	rs143767330	0.03649
NM_007327.4(GRIN1):c.968+151C>T	rs189021406	0.02004
NM_007327.4(GRIN1):c.672-324G>A	rs149867237	0.01481
NM_007327.4(GRIN1):c.1548G>A (p.Pro516=)	rs75783429	0.00518
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=)	rs116006955	0.00510
NM_007327.4(GRIN1):c.768G>C (p.Gly256=)	rs141473515	0.00059
NM_007327.4(GRIN1):c.1513C>T (p.Leu505=)	rs139637382	0.00051
NM_007327.4(GRIN1):c.1331C>T (p.Pro444Leu)	rs200225692	0.00026
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=)	rs145176345	0.00023
NM_007327.4(GRIN1):c.394-4G>A	rs202180269	0.00009
NM_007327.4(GRIN1):c.264C>T (p.Tyr88=)	rs199679287	0.00001
NM_007327.4(GRIN1):c.1340-17delinsGTAA	rs2131292306
NM_007327.4(GRIN1):c.1468-219_1468-204del	rs36070681
NM_007327.4(GRIN1):c.1632+17_1632+23del	rs756425137
NM_007327.4(GRIN1):c.393+327_393+337del	rs56085663
NM_007327.4(GRIN1):c.394-188_394-130del	rs1564344660
NM_007327.4(GRIN1):c.571-1141G>A	rs10870198
NM_007327.4(GRIN1):c.672-106A>C	rs28507734
NM_007327.4(GRIN1):c.672-267_672-229del	rs755849037
NM_007327.4(GRIN1):c.672-330A>G	rs115011370

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