List of variants in gene GRIN1 reported as uncertain significance for not specified

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_007327.4(GRIN1):c.768G>C (p.Gly256=)	rs141473515	0.00059
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=)	rs145176345	0.00023
NM_007327.4(GRIN1):c.1340C>A (p.Pro447His)	rs587780348	0.00014
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=)	rs146086141	0.00004
NM_007327.4(GRIN1):c.1437G>A (p.Val479=)	rs797045604	0.00001
NM_007327.4(GRIN1):c.2170A>T (p.Asn724Tyr)	rs766459225	0.00001
NM_007327.4(GRIN1):c.255C>T (p.Ser85=)	rs797045605	0.00001
NM_007327.4(GRIN1):c.1036C>T (p.Arg346Trp)	rs1833355927
NM_007327.4(GRIN1):c.1339+7GCGCGGGGCAGGGCGCGGG[3]	rs761110882
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu)	rs1328780843
NM_007327.4(GRIN1):c.2054A>G (p.Lys685Arg)
NM_007327.4(GRIN1):c.334G>A (p.Gly112Ser)	rs762157647
NM_007327.4(GRIN1):c.381C>A (p.Ile127=)	rs368378783

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